thesential c buy online: hromato contact us: gr phy s this ... columns catalog.pdf · zorbax...

Your Essential Resource for Columns & SuppliesLC & LC/MS

For more information

Buy online:www.agilent.com/chem/store

Contact us:www.agilent.com/chem/contactus

Scan the QR codewith your smartphonefor more information

THE ESSENTIAL CHROMATOGR

PHY & SPECTROSCOPY CATALOG

LC AND LC/MSThis information is subject to change without notice.

© Agilent Technologies, Inc. 2012Printed in Canada October 31, 20125991-1059EN

204

Whether�you�are�performing�conventional�or�ultra-fast�chromatography,�separating�biomolecules,�or�analyzing�complex�basic�compounds,�you�can�trust�Agilent�for�the�industry’s�highest-performing�columns�that�deliver�the�fast,�reproducible�results�you�need�–�all�engineered�with�Agilent’s�unparalleledquality�and�reliability.

• ZoRBaX Eclipse Plus columns –�C18�and�C8�columns�deliver�superior�peak�shape,�while�thephenyl-hexyl�bonded�phase�and�C18�bonded�phase�for�PAH�separations�expand�selectivity�options�formore�applications.�All�Eclipse�Plus�phases�are�available�in�Fast�LC/UHPLC�RRHD�and�RRHT�columns,1.8�µm.�For�scalability,�the�Eclipse�Plus�C18�phase�is�very�similar�to�the�Poroshell�120�EC-C18�phase.

• In�addition�to�Poroshell�120�and�RRHD�columns,�ZoRBaX Rapid Resolution High Throughput(RRHT) columns are�a�third�Fast�LC�option�with�over�140�1.8�µm�columns�choices.�RRHT�columnsare�available�in�2.1,�3.0�and�4.6�mm�ids,�all�with�600�bar�stability.

And�remember,�when�you�choose�Agilent�ZORBAX�LC�columns,�you�get�more�than�just�a�dependableproduct.�You�also�get�over�40�years�of�expertise�–�along�with�unmatched�technical�support�–�from�theworld’s�largest�chromatography�supplier.�On�the�web,�by�phone�or�in�person,�Agilent�helps�you�solve�the�problems�that�can�slow�you�down�and�get�in�the�way�of�your�results.

The�largest�portfolio�of�Fast�LC�columns,�and�a�broad�family�of�phases�across�all�particle�sizesfor�exceptional�flexibility�and�scalability�

• ZoRBaX Rapid Resolution High definition (RRHd) columns –�1.8�µm�columns�feature�improvedpacking�processes�to�achieve�stability�up�to�1200�bar�for�use�with�the�Agilent�1290�Infinity�LC�andother�UHPLC�instruments�and�are�available�in�more�than�14�phases,�plus�HILIC.

LC and LC/MS Columns

• Poroshell 120 columns –�high�efficiency�and�high�resolution�with�up�to�50%�less�pressure�than�sub-2�µm�columns.

LC and LC/MS CoLuMnS

205www.agiLEnT.CoM/CHEM/LC

CoLuMnS FoR SMaLL MoLECuLE SEPaRaTionS

Table�of�ContentsLC and LC/MS Columns for Small Molecule SeparationsHPLC Column Selection....................................................206Fast Columns for Reversed-Phase HPLC/uHPLC.........227

Poroshell 120 ......................................................................228ZORBAX Rapid Resolution High Definition 1.8 µm......233ZORBAX Rapid Resolution High Throughput 1.8 µm......239Agilent UHPLC Guards......................................................246

Columns for Reversed-Phase analytical HPLC.............247ZORBAX Eclipse Plus........................................................248ZORBAX Eclipse PAH........................................................254ZORBAX Eclipse XDB........................................................256ZORBAX 80Å StableBond.................................................264ZORBAX Rx .........................................................................272ZORBAX 80Å Extend-C18.................................................274ZORBAX Bonus-RP............................................................278ZORBAX Original Reversed-Phase Columns.................283Kits for Analytical HPLC ...................................................284Pursuit..................................................................................287Polaris ..................................................................................298TC-C18(2) and HC-C18(2) .................................................304PLRP-S .................................................................................306

Preparative HPLC Columns..............................................311Agilent Prep LC Columns .................................................311ZORBAX PrepHT ................................................................314Pursuit and Pursuit XRs Prep ..........................................319Polaris Prep Columns........................................................321Load & Lock ........................................................................322Columns for Other HPLC Techniques.............................323ZORBAX HILIC Plus...........................................................324Normal-Phase Columns....................................................326ZORBAX Ion-Exchange Columns – SAX and SCX.........333Hi-Plex Columns for Carbohydrate Analysis .................335

appendices.........................................................................343Quick Guide to USP Designations for HPLC Columns..............................................................343

oligo Solutions ..................................................................347StratoSpheres DNA Cartridges .......................................347TOP, TOP-DNA and TOP-RNA Cartridges ......................348

206


HPLC Column SelectionTo�use�the�column�selection�guide�diagram�below,�simply�follow�the�path�for�your�analyte�and�mobile�phase.�At�the�far�right,�follow�your�final�columnselection�to�the�pages�indicated.

Normal-Phase Mode with Bare Silica

Normal-Phase Mode with Bonded Phase

Reversed-Phase Mode with Bonded Phase

Gel Permeation (Small Molecule)

Reversed-Phase Mode with Bonded Phase

Reversed-Phase Mode with Bonded Phase Using Ionization Control

Reversed-Phase Mode with Bonded Phase Using Ion-Pair Agent

Reversed-Phase Mode with Bare Silica (HILIC)

Ion-Exchange Mode

Gel Permeation Chromatography

Gel Filtration Chromatography

Ion-Exchange Mode with Wide-Pore Material

Reversed-Phase Mode with Wide-Pore Material

Molecular Weight< 3000

Hexane Soluble

Ionic

Non-Ionic

MeOH and MeOH:H2O or ACN and

ACN: H2O Soluble

THF Soluble

Molecular Weight> 3000

Page 333

Page 247

Page 324

Page 247

88

Page 248

Pages 326-328

Pages 326-328

Adapted�with�permission�from�"Practical�HPLC�Methodology�and�Applications,"�Brian�A.�Bidlingmeyer,�John�Wiley�&�Sons,�Inc.,�New�York,�p.�109

Sample

Size Exclusion Chromatography

Page 523

Organic SolventSoluble

Water Soluble

Water Soluble

Organic SolventSoluble

BioMoLECuLES

Information�about�biocolumns�with�molecular�weight�>�3000�can�befound�in�the�Agilent�BioHPLC�Column�section,�turn�to�page�350.

Page 523

Page 248

Page 488

Page 431

Page 397



(Continued)

Quick guide to agilent Reversed-Phase Bonded Phases

ZoRBaX RP-HPLC Columns Recommended uses and applications Page no.Poroshell�120 ü Superficially�porous�particles�for�high�efficiency�at�low�pressure

ü Sub-2�µm�efficiency�with�a�2.7�µm�particleü Endcapped�and�non-endcapped�C18�and�C8�phases,�and�a�variety�of�other�phases,�for�selectivity�optimization

ü Compatible�with�400�bar�and�600�bar�LC's

228

Eclipse�PlusAvailable�in�RRHD�(1200�bar)�and�RRHT�(600�bar)�configurations,�1.8�µm

ü Excellent�first�choice�for�method�developmentü Long�life�from�pH�2-9�for�reliable�separations�of�basic,�acidic�and�neutral�compoundsü Superior�peak�shape�with�basic�compoundsü High�resolution�and�efficiency�with�1.8,�3.5�and�5�µm�columnsü Rigorous�QA/QC�testing�for�greater�long-term�reproducibility

248

Eclipse�XDBAvailable�in�RRHD�(1200�bar)�and�RRHT�(600�bar)�configurations,�1.8�µm

ü Four�selectivity�choices�for�flexible�method�developmentü High�performance�over�a�wide�pH�range�(2-9)ü Good�peak�shape�for�acids,�bases�and�neutralsü Long�lifetime�with�eXtra�Dense�Bonding�and�double�endcappingü Fast,�ultra-fast,�and�high�resolution�separations�using�1.8�and�3.5�µm�columnsü Choices�from�capillary�to�prep

256

StableBond�(SB)Available�in�RRHD�(1200�bar)�and�RRHT�(600�bar)�configurations,�1.8�µm

ü Basic,�acidic,�neutral�compoundsü Exceptional�stability�at�low�pH�(1-2)ü Use�of�high�temperature�(up�to�90�°C�for�C18,�80�°C�for�C8,�C3,�Phenyl,�CN,�and�Aq)�and�low�pH�as�an�added�selectivity�tool

ü Widest�selection�of�bonded�phases�for�different�selectivity�(C18,�C8,�C3,�CN,�Phenyl,�Aq)ü Uses�mobile�phases�for�LC/MS�with�formic�acid,�acetic�acid,�or�TFAü Uses�mobile�phases�with�TFA�for�peptide�and�protein�separationü Rapid�separations�using�1.8�and�3.5�µm�columns

264

Information about biocolumns can be found in the section beginning on page 350

208


TiPS & TooLS

ZORBAX�RxAvailable�in�RRHD�(1200�bar)�and�RRHT�(600�bar)�configurations,�1.8�µm

ü General�separation�of�basic,�acidic�and�neutral�compounds�at�low�pH�with�different�selectivitythan�SB�columns

ü Rx-C8�is�the�same�as�SB-C8

272

Bonus-RPAvailable�in�Fast�LC/UHPLC�RRHD�(1200�bar)and�RRHT�(600�bar)�configurations,�1.8�µm

ü Separating�basic�compounds�in�higher�aqueous�mobile�phasesü General�separation�of�basic,�neutral,�acidic�compounds�at�mid-range�pH�or�low�pH;�especially�stable�at�low�pH

ü Separating�peptides�for�different�selectivityü Rapid�separations�using�3.5�µm�columns

278

Extend-C18Available�in�Fast�LC/UHPLC�RRHD�(1200�bar)and�RRHT�(600�bar)�configurations,�1.8�µm

ü Separating�basic�compounds�above�their�pKa�in�free�base�form;�separation�of�basic,�acidic,neutral�compounds�at�high�pH;�up�to�pH�11.5

ü Uses�ammonium�hydroxide�as�mobile�phase�additive�with�LC/MS�with�small�molecules�or�peptides

ü Separating�at�high,�mid-range�and�low�pH�for�selectivity�changesü Rapid�separations�using�3.5�µm�columns

274

original ZoRBaX Columns Recommended uses and applications Page no.ZORBAX ü General�separation�of�basic,�acidic,�neutral�compounds�at�low�pH�with�different�selectivity

than�SB�columns;�higher�number�of�active�silanols�than�SBü "Mixed�mode"�separation�at�more�neutral�pH�valuesü Available�in�ODS,�C8,�CN�and�ODS�"Classic"�(non-endcapped)

283

ZoRBaX RP-HPLC Columns Recommended uses and applications Page no.

Quick guide to agilent Reversed-Phase Bonded Phases

The LC Handbook: guide to LC Columns and Method development

This�handy�guide�makes�it�easy�to�choose�the�right�LC�column,�and�contains�plenty�of�tips�and�tricks�to�makeyour�job�easier�and�more�productive�(publication�#�5990-7595EN).

Request a copy or download a mobile copy at www.agilent.com/chem/lchandbook



Quick guide to additional agilent Reversed-Phase Columns

Pursuit Family Recommended uses and applications Page no.Pursuit�HPLC ü Full�range�of�phases,�including�C18�and�C8

ü Diphenyl�utilizes�strong�dipole-dipole�hydrogen�bonding�and�pi-pi�mechanisms�for�differentselectivity�with�aromatic�compounds

ü PFP�provides�excellent�separation�of�polar�(halogenated)�analytes�and�positional�isomers�understandard�reversed-phase�conditions

287

Pursuit�XRs�and�Pursuit�XRs�Ultra ü Offer�larger�surface�area�and�smaller�pore�size,�in�complementary�phases�to�Pursuit�familyü Ultra�offers�stability�to�600�bar,�due�to�special�hardware�and�loading

287

Polaris Family Recommended uses and applications Page no.C18-A�and�C8-AAvailable�in�3.0,�5.0,�and�10�µm�(C18-A�only)

ü C18-A�and�C8-A�offer�alternate�selectivities�for�general�polar�applicationsü Designed�with�hydrogen-bond-accepting�endcapping

298

Amide-C18Available�in�3.0�and�5.0�µm�

ü Subtle�alternative�selectivity�due�to�the�absence�of�steric�protectionü Utilize�an�embedded�amide,�similar�to�ZORBAX�Bonus-RP

298

C18-Ether�and�C8-Ether�Available�in�3.0�and�5.0�µm

ü Endcapped�with�an�ether�group�to�create�a�more�polar�surface�for�selectivity�variation 298

other agilent Columns Recommended uses and applications Page no.TC-C18(2)Available�in�5�µm

ü An�excellent�choice�for�mixtures�of�polar�and�non-polar�compounds,�including�strong�basic�compounds

304

HC-C18(2)Available�in�5�µm

ü High-value,�highly�retentive�optionü Carbon�load�of�17%ü Superior�peak�shape�for�basic�compounds

304

210


ZORBAX Reversed-Phase HPLC Column Selection Flow ChartFor small and large moleculesMost�chromatographers�use�reversed-phase�HPLC�as�one�of�their�key�analysis�techniques.�Reversed-phase�HPLC�can�be�used�to�analyze�ionic�and�nonionicanalytes.�Therefore�this�ZORBAX�Column�Selection�Flow�Chart�will�focus�on�reversed-phase�columns.�To�more�easily�select�a�reversed-phase�column�formethod�development�of�small�and�large�molecules,�follow�the�outline�on�these�pages.

This�flow�chart�provides�information�on�choosing�an�initial�column�for�method�development�of�small�molecule�and�protein�and�peptide�samples,�and�includesdecisions�on�bonded�phase�and�column�configuration.

* First�choice�for�use�on�the�1290�Infinity�LC�or�other�UHPLC�instruments�with�1000+�bar�pressure�limit.

First choice of a packing pore size is based on the size of molecules to be analyzed. Typical small molecules can diffuse easily in and out ofstandard 80-120Å pore packings, but larger peptides and proteins may not. For this reason, it is recommended to use 300Å pore packings (300SB)

for isocratic or gradient separations of peptides and proteins.

MW < 3000 MW > 3000

Eclipse Plus C18 or Poroshell 120 EC-C18

StableBond 300SB-C18

A C18 is recommended as the starting column bonded phase for most samples since it maximizes retention for moderately polar to non-polarcompounds. Shorter chain phases should be considered if resolution cannot be optimized with a C18 phase or if you are analyzing larger proteins,

or very hydrophobic compounds that are difficult to elute from C18 with conventional reversed-phase solvents. Start with Poroshell 120 EC-C18 or Eclipse Plus RRHT/RRHD for fast LC performance.

Small Molecules Large Molecules

Starting Column Bonded Phase

Packing Pore Size80-120Å 300Å

MW < 3000 MW > 3000Small Molecules Large Molecules

4.6 x 150 mm, 3.5 µm959963-902

4.6 x 75 mm, 2.7 µm697975-902

4.6 x 100 mm, 2.7 µm695975-902

2.1 x 50 mm, 1.8 µm959757-902

4.6 x 150 mm, 5 µm883995-902

4.6 x 50 mm, 3.5 µm865973-902

2.1 x 75 mm, 5 µm660750-902

ZoRBaX 300SB-C18

Fast analysisStandard analysisStandard analysis

Eclipse Plus C18

Poroshell 120 EC-C18

Fast analysis

Poroshell 120 EC-C18

ZoRBaX RRHd* Eclipse Plus C18

ZoRBaX RRHd 300SB-C18

Poroshell 300SB-C18

Information about biocolumns can be found in the section beginning on page 350



Column and Mobile Phase Guidelines: Reversed-PhaseHPLC�columns�consist�of�two�parts:�the�column�chemistry�and�hardware.�For�the�proper�column�chemistry,consult�the�catalog�section�for�each�type�of�bonded�phase.�For�choosing�column�hardware�and�particlesizes,�consult�the�section�on�column�sizes�and�rapid�separations,�including�Agilent�ZORBAX�Rapid�Resolution�HT,�Solvent�Saver,�Capillary�and�PrepHT�columns.

Pore Size SelectionChoose�a�column�packing�with�small�pore�(60-120Å)�if�the�solute�molecular�weight�is�less�than�about�3000.Otherwise,�use�column�packing�with�the�300Å�pore�size.

Particle Size SelectionThe�typical�particle�size�for�HPLC�columns�is�5�µm�with�3.5�µm�and�smaller,�now�common�in�methoddevelopment.�If�high-speed�analyses�or�higher�resolution�analyses�are�required,�packing�with�1.8�µm�and�2-3�µm�particles�can�be�used.�Shorter�columns�with�these�particles�can�produce�faster�high-resolutionseparations,�with�the�1.8�µm�particle�size�providing�the�highest�efficiency�and�2.7�µm�superficially�porousproviding�similar�results.�With�1.8,�2.7,�3.5�and�5�µm�particle�sizes�to�choose�from,�start�with�the�smallestparticle�size�for�your�HPLC�or�UHPLC�–�400�bar,�600�bar,�or�1200�bar�–�to�achieve�the�best�results.

Column ConfigurationChoosing�the�best�column�size�for�method�development�has�changed�dramatically�in�the�past�few�years.Smaller�3.0�mm�id�or�2.1�mm�id�columns�are�now�used�more�than�4.6�mm�id�to�lower�solvent�use�andachieve�compatibility�with�MS�detectors.�And�shorter�50,�75�and�100�mm�long�columns�can�be�a�greatstarting�choice,�with�longer�columns�used�only�when�more�resolution�is�needed�or�when�3.5�and�5�µmparticle�sizes�are�used.

ZORBAX�Rapid�Resolution�High�Throughput�(RRHT)�Columns

Need�help�selecting�the�right�LC�column�for�your�method?�Try�the�Navigator:�A�selection�tool�for�LC�columns�and�sample�prep.�Look�for�it�online�and�via�your�mobile�device�at�http://navigator.chem.agilent.com

TiPS & TooLS

212


Base MaterialThe�base�material�for�an�LC�column�is�most�often�high�purity�silica�material�with�totally�porous�particles�suchas�that�used�in�most�Agilent�columns,�including�ZORBAX,�Pursuit,�and�Polaris.�However,�more�choices�areavailable,�including�polymer�material�with�high�pH�stability�used�in�PLRP-S�columns�and�superficially�poroussilica�particles�such�as�those�used�in�Poroshell�120�columns.�The�high�purity�Type�B�silicas,�including�theZORBAX�Rx-Sil�used�in�ZORBAX�Eclipse�Plus,�and�superficially�porous�Poroshell�120,�are�an�excellent�firstchoice�for�most�methods.�Type�A�silicas,�such�as�ZORBAX�SIL,�used�in�Original�ZORBAX�columns,�are�stillmanufactured�and�used�in�many�methods.

Bonded PhaseA�good�first�choice�for�bonded�phase�is�C18�or�C8,�and�the�recommended�starting�column�choices�areEclipse�Plus�C18�or�Poroshell�120�EC-C18.�These�two�choices�provide�excellent�peak�shape�and�can�beused�over�the�pH�range�2-9,�accommodating�most�typical�LC�and�LC/MS�mobile�phases.�If�the�samplesolutes�of�interest�are�not�adequately�separated�on�these�columns,�CN�and�Phenyl�columns�–�includingPhenyl,�Phenyl-Hexyl�and�Diphenyl�–�may�offer�significant�differences�in�selectivity�from�straight-chain�alkylphases�to�effect�the�separation.

In�general,�larger�solutes,�such�as�proteins,�are�best�separated�on�short-chain�reversed-phase�columns�(C3,�CN,�C8)�and�peptides�and�small�molecules�are�separated�on�longer-chain�columns�(C18).�However,there�are�many�cases�where�this�conventional�wisdom�does�not�apply.�For�example,�peptides�can�also�beeffectively�separated�using�short-chain�columns,�and�hydrophobic�peptides�can�show�better�recovery�on�longer-chain�phases.�Therefore,�it�is�best�to�initially�select�a�phase�in�the�middle�of�the�hydrophobicspectrum�(e.g.,�C8),�then�change�to�a�more�hydrophobic�phase�or�more�hydrophilic�phase�depending�oninitial�results�and�solubility�properties�of�your�sample.

PolymersWhen�a�column�is�needed�that�can�operate�at�very�low�and�very�high�pH,�polymeric�packings�provide�an�alternative�to�silica-based�materials.�Polymeric�particles�are�good�for�small-scale�chromatography,particularly�LC/MS,�as�they�are�chemically�stable�and�do�not�leach�soluble�or�particulate�species.��Reversed-phase�spherical�polymeric�packings�used�in�Agilent�PLRP-S�columns,�for�example,�are�based�on�astyrene/divinylbenzene�copolymer�with�an�inherently�hydrophobic�surface.�No�bonded�phase�is�required�forreversed-phase�chromatography�with�polymeric�particles.�These�rigid�macroporous�particles�can�be�coatedand�derivatized�to�give�a�range�of�functionalities,�including�weak�and�strong�cation�and�anion�exchangers.

Silica, Polymers, and Bonded Phase



pH and Mobile PhaseThe�choice�of�mobile�phase�for�a�reversed-phase�system�starts�with�selecting�the�organic�modifier.Acetonitrile�is�the�most�commonly�used�organic�modifier.�However,�selectivity�differences�and�sampleretention�will�vary�significantly�among�mobile�phases�containing�acetonitrile,�methanol,�and�tetrahydrofuran(THF).�Sample�solubility�is�likely�to�differ�in�such�solvents�and�dictate�use�of�a�specific�solvent�or�solvents.�UV�detection�at�certain�wavelengths�is�not�possible�with�certain�modifiers�(e.g.,�methanol�at�200�nm).

Both�pH�and�ionic�strength�of�the�aqueous�portion�of�mobile�phases�are�important�parameters�in�developingrugged�methods�that�are�not�sensitive�to�small�variations�in�conditions.�With�ionic�compounds,�retention�oftypical�species�shows�significant�changes�with�pH.�It�is�very�important�to�control�pH�in�such�reversed-phasesystems�to�stabilize�retention�and�resolution.�A�pH�between�2�and�4�generally�provides�the�most�stableconditions�for�retention�vs.�small�changes�in�pH,�and�this�pH�is�recommended�for�starting�methoddevelopment�for�most�samples,�including�basic�compounds�and�typical�weak�acids.

HPLC Column

Stationary Phase

Type�ofSurface Pore�Size Particle�

Size

Column dimensions

Length InnerDiameter

Chemical PropertiesChemical�Lifetime/Selectivity

Retention�Factor

Physical PropertiesEfficiencySensitivitySpeed

214


Working with LC/MS

Since�many�LC/MS�analyses�are�run�at�lower�flow�rates�(typically�from�µL/min�flow�rates�up�to�1�mL/min),moving�to�smaller�internal�diameter�columns�is�the�best�choice�for�the�user.�Agilent’s�Solvent�Saver�(3.0�mm�id)�and�narrow�bore�(2.1�mm�id)�will�often�result�in�lower�solvent�usage�for�the�method,�and�are�excellent�options�for�high�resolution�and�higher�sensitivity�than�the�larger�id�columns.

Most�often,�the�best�bonded�phase�choice�is�an�endcapped�C18�phase.�Eclipse�Plus�C18�is�a�highperformance�endcapped�C18�phase�available�in�sub-2�µm�RRHD�and�RRHT�column�formats.�For�fast�high-throughput�separations�with�LC/MS,�Poroshell�120�EC-C18�is�an�excellent�choice.�Poroshell�has�a�larger�frit,�so�it’s�well�suited�for�dirtier�LC/MS�samples,�such�as�blood�plasma,�which�may�often�clogcolumns�with�smaller�porosity�frits.��

Both�Eclipse�Plus�C18�and�Poroshell�120�EC-C18�phases�are�stable�over�a�wide�pH�range�and�arecompatible�with�the�volatile�buffers�such�as�acetic�and�formic�acids.

TiPS & TooLS

LC Flow Rate Calculator app

This�FREE�Smartphone�app�lets�you�quickly�adjust�your�flow�rate�to�accommodate�other�method�changes.

Download�at�www.agilent.com/chem/lcapp

When�choosing�HPLC�columns�for�LC/MS,�chromatographers�often�need�to�consider�several�aspects�oftheir�method�and�separation,�typically�including�resolution,�flow�rate,�and�stationary�phase�choice.�Often,�for�relatively�simple�analytes,�shorter�high�resolution�columns�are�the�best�choice.�These�columns�allow�forhigh�throughput�while�maintaining�high�separation�efficiency.�Narrow�bore�Rapid�Resolution�High�Definition(RRHD)�for�separations�(>�600�bar)�and�Poroshell�120�columns�(<�600�bar)�offer�high�resolution�even�inshorter�columns�dimensions.�For�more�difficult�samples,�users�should�seek�longer�column�lengths.



Transferring your method to a high efficiency columnHigh�efficiency�columns�for�UHPLC/Fast�LC�will�help�you�increase�your�analytical�speed�and�resolution.Depending�on�the�instrument�configuration�you�are�using,�you�may�need�to�make�a�few�adjustments�to�get�the�most�from�these�columns.

Because�of�their�high�efficiency,�very�narrow�peaks�elute�from�higher�efficiency�columns�quickly.�While�modern�HPLC�instrumentation�and�data�systems�are�able�to�capture�the�benefits�of�these�particles,attention�to�instrumental�configuration�is�important�to�get�the�best�results.�

Steps�to�transfer�your�method:

Check the specifications that came with your instrument –�Your�instrument�may�already�beconfigured�appropriately�for�high�efficiency�columns.�If�not,�then�continue.

optimize the data collection rate for LC and LC/MS (at least 40 Hz detector with fastresponse time for uV) –�Set�the�detector�to�the�fastest�setting,�then�to�the�second�fastest�setting�and�evaluate�if�the�resolution�is�different.�

TiPS & TooLS

For�the�Agilent�1290�Infinity�LC,�in�situations�requiring�extremely�low�dead�volumes,�use�the�ultra-low�dispersion�kit,�which�includes�an�ultra-lowdispersion�flow�cell�and�0.08�mm�id�capillaries.

use a semi-micro or micro-flow cell –�Smaller�volume�flow�cells�such�as�the�semi-micro�(6�mm/5�µL)or�micro�(3�mm/2�µL)�are�recommended�for�best�performance.�There�are�newer�cartridge�flow�cells�(e.g.�the�Ultra�Low-Dispersion�Max-Light�Ultra�Flow�Cell,�P/N�G4212-60007)�designed�to�optimize�UHPLC�instrument�performance.

216


Minimize injection sample dispersion in the column –�Use�an�injection�solvent�with�solvent�strengththat�is�equivalent�to�or�weaker�than�the�mobile�phase,�especially�when�using�an�isocratic�method.�This�isgood�practice�in�general�for�any�column,�and�more�important�with�high�efficiency�columns.

Scale your gradient profile and injection volume –�If�using�gradient�elution,�scale�the�gradient�profile�and�injection�volume�to�the�new�smaller�column�to�quickly�transfer�the�method�and�avoidoverloading.�For�isocratic�and�gradient�elution,�make�sure�that�you�scale�the�injection�volume�to�match�the�overall�column�volume.

Minimize tubing volume in the instrument –�Use�Red�(0.12�mm�id)�tubing�instead�of�Green�(0.17�mm�id)�as�it�has�only�half�of�the�volume�that�the�sample�has�to�travel�through.�This�cuts�down�extra�column�band�broadening.�Ensure�that�your�connections�are�as�short�as�possible.�The�key�locations�to�check�are:

TiPS & TooLS

See�a�video�that�takes�you�through�these�steps�at�www.agilent.com/chem/poroshell120video

Also,�check�out�the�LC�Method�Translator�Tool�at�www.agilent.com/chem/lcmethodtranslator

• The�autosampler�needle�seat• The�autosampler�to�the�Thermostatted�Column�Compartment�–�or�‘TCC’• The�TCC�to�the�column• The�column�to�the�flow�cell,�including�the�internal�diameter�of�the�integral�flow�cell�inlet�capillary

Turn to pages 36-39.

all of these specific capillaries can be ordered individually from agilent, in the lengths you need, and for your instrument.



1200�bar�removable�fitting�(SV),�5067-4733

optimize your flow rate –�For�Poroshell�120,�if�you’re�using�a�2.1�mm�id,�the�suggested�starting�flow�rate�is�0.42�mL/min;�for�3.0�mm�id�Poroshell�120�columns,�we�suggest�starting�at�0.85�mL/min,�and�for�4.6�mm�id,�we�suggest�starting�at�1.5�-�2�mL/min.

VHP FiTTingS

min0 1 2 3 4 5 6 7 8 9

mAU

0

10

20

0.69

6 0

.816

0.98

8

1.81

9

2.15

2

5.19

0

8.74

1

min0 1 2 3 4 5 6 7 8 9

mAU

0

10

20

0.47

3 0

.544

0.65

9

1.20

2

1.42

1

3.43

9

5.82

5

min0 1 2 3 4 5 6 7 8 9

mAU

0

10

20

0.41

9 0

.510

0.95

4

1.14

8

2.68

7

4.42

85

5

5

15

15

151

2

3 4

5

Fast analysis of cefepime and related impuritiesColumn: Poroshell 120 EC-C18

697975-9024.6 x 75 mm, 2.7 µm

Instrument: Agilent�1200�Infinity�Series�Rapid�Resolution�LC�System

Detector: DAD,�254�nm

1. Impurity�E2. Cefepime3. Impurity�F4. Impurity�A5. Impurity�B

1.5�mL/min225�bar

2.0�mL/min300�bar

1�mL/min155�bar

Agilent’s�1200�bar�removable�fitting�(for�1/16�in�od�capillaries)�consists�of�a�stainless�steel�screw,�an�internal�stainless�steelferrule�and�a�front�ferrule�in�PEEK.�The�fitting�can�be�used�throughout�the�flow�path,�but�because�it�can�be�re-used�withoutlosing�tightness,�it�is�especially�suitable�for�the�connection�between�the�heat�exchanger�and�the�column.�This�new�andimproved�fitting�replaces�the�standard�stainless�steel�Swagelok�fitting�which�was�not�removable.�The�Very�High�Pressure(VHP)�fitting�is�available�in�three�sizes�–�short�(P/N�5067-4733),�long�(P/N�5067-4738)�and�extra�long�(P/N�5067-4739).The�short�fitting�is�the�one�that�is�most�commonly�used,�and�will�be�appropriate�90%�of�the�time.�In�some�cases,�if�usingcolumns�with�longer�nuts,�a�longer�fitting�will�be�needed.

Take care to make proper connections –�Agilent�recommends�Swagelok�fittings�with�front�and�backferrules,�which�give�best�sealing�performance�throughout�our�LC�system�(use�this�on�the�instrumentconnections,�i.e.�valves,�heaters,�etc).�Polyketone�fittings�are�highly�recommended�for�up�to�600�bar.�Usethis�fitting�(P/N�5042-8957)�on�column�connections�with�Poroshell�120.�For�RRHD�columns,�use�Agilent'sremovable�1200�bar�fitting�(P/N�5067-4733).

218


Start with Poroshell 120 for Fast LC performance on any HPLC – phases align with ZoRBaX family.

up to 50% less pressure than sub-2 µm; a total lab productivity enhancer

**Best Phase for Method development

1.7 µm solid core; 0.5 µm porous outer layer for a 2.7 µm particle, id's: 4.6 mm, 3.0 mm, 2.1 mm, Lengths: 30-150 mm.New phases coming soon! Check www.agilent.com/chem/poroshell120

Compatible with HPLC and UHPLC instruments. Suitable for analysis of acids, bases, and neutrals. Also great for peptide mapping.Poroshell 120 is for any lab looking for increased analytical speed and resolution with less backpressure.

Poroshell 120

ZoRBaX Family

ZoRBaX StableBond

R

R

R

R

R

R

R1SiO

OH

OH

R1SiO

R1SiO

CH3

CH3

Si

CH3

CH3

CH3Si

CH3

CH3

CH3Si

CH3

CH3

Si

CH3

CH3

Si

O

O

O

O

O

CH3

CH3

Si

CH3

CH3

CH3Si

CH3

CH3

CH3Si

CH3

CH3

Si

CH3

CH3

Si

O

O

O

O

O

SB-C18 (USP L1),SB-C8 (USP L7),SB-C3 (USP L56),

SB-Phenyl (USP L11),SB-Cn (USP L10),

SB-aq

RRHd: 1.8 µm, stable to 1200 bar;RRHT: 1.8 µm, 600 barLengths: 20-250 mm

IDs: 4.6 mm , 3.0 mm, 2.1 mm, 1.0 mm; Prep, Capillary (C18)

High performance with acids, bases, andneutrals with superior lifetime at low pH.

Sample applicationsChemical/industrial: Triton

Environmental: Organic acids, pesticides in drinking waterFood Safety: Anthocyanine,

parabenes, melaminePharmaceutical: Analgesics,

anesthetics, traditional Chinese medicine

non-EndcappedTemp limit: 80 °C (90 °C for SB-C18)Pore size: 80ÅSurface area: 180 m2/gParticle sizes: 1.8, 3.5, 5, 7 µm

pH: 1.0-8.0 (0.8-8.0 for SB-C18)Carbon Load: C18: 10%; C8: 5.5%;C3: 4%; Phenyl: 5.5%;CN: 4%, Aq: Proprietary

Best for low pH mobile phases – great for method development

ZoRBaX Eclipse Plus**

C18 (USP L1),C8 (USP L7),

Phenyl-Hexyl (USP L11),PaH (USP L1)

High performance and excellent peak shapewith acids, bases and neutrals.

Sample applicationsEnvironmental: EPA Method 1694,

Illicit and prescribed drugs in wastewaterFood Safety: Quinolone antibioticsPharmaceutical: Chloramphenicol,Simvastatin, Chrysophenol (TCM),

amphetamine, ranitidine

double Endcapped(except PAH, which is not endcapped)Temp limit: 60 °CPore size: 95ÅSurface area: 160 m2/g

Particle sizes: 1.8, 3.5, 5 µmpH: 2.0-9.0 for C18,C8; 2.0-8.0 for PAH,Phenyl-HexylCarbon load: C18: 9%; C8: 7%;Phenyl-Hexyl: 9% ;PAH: 14%

Best all around – exceptional peak shape,efficiency, resolution, and lifetime

ZoRBaX Eclipse XdB

C18 (USP L1),C8 (USP L7),

Phenyl (USP L11),Cn (USP L10)

Good peak shape for basic, acidic, andneutral compounds with high performanceover a wide pH range (pH 2-9). eXtra DenseBonding and double endcapping help give

this column a long lifetime.

Sample applicationsEnvironmental: Herbicides/pesticides,

steroids in waterFood Safety: Food colors,

aromatic flavorings, mycotoxins,epoxyphenolic-based can coatings

Pharmaceutical: Goldenseal and relatedalkaloids, antidepressants, triamcinolone

double EndcappedTemp limit: 60 °CPore size: 80ÅSurface area: 180 m2/gParticle sizes: 1.8, 3.5, 5, 7 µm

pH: 2.0-9.0 (2.0-8.0 for CN)Carbon load: C18: 10%; C8: 7.6%;Phenyl: 7.2%; CN: 4.3%

High performance over a wide pH range


IDs: 4.6 mm, 3.0 mm, 2.1 mm, 1.0 mm;Capillary and Prep

Pursuit/Pursuit XRs

C18 (USP L1), C8 (USP L7), diphenyl (USP L11), PFP (USP L43),

PaH (USP L1), Si (USP L3)

Pursuit XRs offers higher loadability and Pursuit XRs Ultra is loaded for higher pressure stability.

Endcapped(except Pursuit XRs Si)Pore Size: 200Å(Pursuit), 100Å (Pursuit XRs)Surface area: 200 m2/g(Pursuit); 440 m2/g(Pursuit XRs)Particle Sizes: 3, 5, 10 µm

pH: 2.0-9.0Carbon Load: Pursuit C18: 12.9%;Pursuit C8: 7.4%;Pursuit Diphenyl: 7.3%;PFP: 6.3%; XRs C18: 22%; XRs UltraC18: 23.3%; XRs UltraC8: 15%; XRs UltraDiphenyl: 14.6%

Reliable Selectivity alternatives

Lengths: 30-250 mmIDs: 2.0 mm, 3.0 mm, 4.6 mm; Prep

agilent LC Columns overview: Small Molecules

Poroshell 120 EC-C18** (uSP L1), EC-C8** (uSP L1), Phenyl-Hexyl (uSP L11)

Carbon Load: Phenyl-Hexyl - 8%Poroshell 120 SB-C18 (uSP L1), SB-C8

Carbon Load: SB-C18 - 7.5%, SB-C8 - 4.5% Poroshell 120 EC-Cn (uSP L10)


IDs: 4.6 mm, 3.0 mm, 2.1 mm, 1.0 mm; Prep



Poroshell 120 SB-aQCarbon Load: Proprietary

HOOH

O

OO

O

N

HON

N

O

R1

CH3

CH3

CH3

CH3

CH3

CH3

Si

SiO

O

O PG

PG

PG

R

R

R

Si

Si

Si

R1

R1

R1

R1

R1

OSi

C18

C18

Silica Support

SiO

ZoRBaX Bonus-RP

Bonus-RP (USP-L60)

PoLaR Compounds

Polar-embedded to improve peak shapes;for basic compounds at low and mid pH.

Sample applicationsEnvironmental: Triazine pesticidesFood Safety: Hydroxymethylfurfural

Pharmaceutical: Antifungal medications,anorectics, ulcer medications


IDs: 4.6 mm, 3.0 mm, 2.1 mm, 1.0 mm; Prep

Triple-EndcappedTemp limit: 60 °CPore size: 80ÅSurface area: 180 m2/gParticle sizes: 1.8, 3.5, 5 µm

pH: 2.0-9.0Carbon load: 9.5%

alternative selectivity to alkyl, phenyl, cyano phases

ZoRBaX Extend-C18

C18 (USP L1)

Sample applicationsEnvironmental: EPA 8330 (explosives)Food Safety: Aflatoxins, mycotoxinsPharmaceutical: Antihistamines,

xanthines

double-EndcappedTemp limit: 60 °CPore Size: 80ÅSurface area: 180 m2/gParticle sizes: 1.8, 3.5, 5 µm

pH: 2.0-11.5Carbon load: 12.5%

a good option for separations at high pH

SB-aQ

ZoRBaX SB-aq

Proprietary phase ideal for polarcompounds and high aqueous conditions.

Sample applicationsEnvironmental: Pesticides in drinking water

Food Safety: Pesticides in foodPharmaceutical: Water-soluble vitamins

See ZORBAX StableBond for specification and structure.

Polaris

C18-a (USP L1), C8-a (USP L7), C18-Ether (USP L1), C8-Ether (USP L7), amide-C18 (USP L60), nH2 (USP L8),

Si-a (USP L3)

Hydrogen-bond accepting and ether groupendcapping provide alternate selectivities.

Sample applicationsEnvironmental: Triazine pesticidesFood Safety: Hydroxymethylfurfural

Pharmaceutical: Antifungal medications,anorectics, ulcer medications

EndcappedPore size: 180ÅSurface Area: 200 m2/gParticle Sizes: 3, 5, 10 µmpH: 2.0-9.0

Carbon load: PolarisC18-A: 13.8%; Polaris C8-A: 7.4%;Polaris C18-Ether:12.1%; Polaris C8-Ether: 7.1%

More options for Polar Compounds

HILIC Plus is a HILIC column based on Eclipse Plus silica for excellent peak shapes

RRHd: 1.8 µm, stable to 1200 barLengths: 50, 100, 150 mmIDs: 4.6 mm (3.5 µm only), 3.0 mm, 2.1 mm

Looking for a HiLiC column?

RRHd: 1.8 µm stable to 1200 bar;RRHT: 1.8 µm, 600 barLengths: 20 - 250 mm

IDs: 4.6 mm, 3.0 mm, 2.1 mm; Prep

Lengths: 30-250 mm, (available in

3 µm and 5 µm particles)IDs: 2.0 mm, 3.0 mm, 4.6 mm; Prep

High efficiency and long life at high pH –up to pH 11.5. Improve retention,resolution and peak shape of basic

compounds. High sensitivity for LC/MSseparations of peptides. Uniquebidendate bonding and double

endcapping provides high pH stability.

Exceptional lifetime at low pH – no endcapping

High sensitivity for LC/MS applications and recommended for EPA 1694.

Poroshell 120 Bonus-RP (uSP L60)Carbon Load - 7.5%


IDs: 4.6 mm, 3.0 mm, 2.1 mm, 1.0 mm

information about biocolumnscan be found in the sectionbeginning on page 350

Endcapped: EC-C18, EC-C8, Phenyl-Hexyl, Bonus-RP (triple), EC-Cnnon-endcapped: SB-C18, SB-C8 and SB-aqTemp Limit: 60 °C (EC-C18, EC-C8, Phenyl-Hexyl, Bonus-RP); 80 °C (SB-C8, SB-Aq); 90 °C (SB-C18)Pore Size: 120Å ; Surface Area: 130 m2/g; pH: 2.0-8.0 (EC-C18, EC-C8, Phenyl-Hexyl); 1.0-8.0 (SB-C18, SB-C8, SB-Aq); 2.0-9.0 (Bonus-RP); Carbon Load: 8% (EC-C18); 7% (EC-C8)

Poroshell 120 HiLiC: 2.7 µm, stable to 600 barnon-bonded silicaPore size: 95Å (120Å, Poroshell 120)Surface Area: 160 m2/g(130 m2/g for Poroshell 120)Particle Sizes: 1.8, 2.7, 3.5 µmpH: 0-8.0

220


Method Development from pH 1-12Start method development at low pH (pH 2-3)With�so�many�column�choices�available,�how�do�you�know�where�to�start�your�method�development?�The�recommended�starting�point�for�methoddevelopment�is�using�a�buffered�low�pH�mobile�phase�–�around�pH�2-3.�Using�a�low�pH�mobile�phase�most�often�results�in�the�best�peak�shape�for�basiccompounds�on�silica-based�columns.�At�low�pH,�the�silanols�on�the�silica�are�fully�protonated�so�positively�charged�basic�compounds�do�not�interact�strongly.The�result�is�good�peak�shape.�Many�acidic�compounds�are�non-charged,�maximizing�their�retention�at�low�pH.�These�observations�are�key�advantages�tomethod�development�at�low�pH.

For�standard�analytical�work,�start�method�development�with�acetonitrile�as�the�mobile�phase�organic�modifier�and�20-50�mM�phosphate�buffer�(pH�2-3)�as�the�aqueous�component�for�non-LC/MS�applications.�These�conditions�provide�good�pH�control,�necessary�for�the�most�reproducible�analyses�of�ionizablecompounds.�For�LC/MS�applications�formic�acid�or�TFA�are�good�mobile�phase�additives�for�low�pH.

Optimize solvents and bonded phases at low pHThe�initial�method�development�steps�may�lead�very�quickly�to�a�satisfactory�separation.�But�if�more�optimization�is�needed,�acetonitrile�can�be�replaced�with�methanol�or�tetrahydrofuran�and�the�separation�re-optimized.�This�step�may�lead�to�a�satisfactory�solution,�but�if�still�more�selectivity�optimization�is�needed,�the�column�bonded�phase�can�be�changed.

At�low�pH�there�are�many�bonded�phase�choices�available�for�optimization.�These�include�the�Eclipse�Plus�phases�as�well�as�the�Eclipse�XDB�family�withC18,�C8,�Phenyl�and�CN.�Alternate�choices�include�five�different�StableBond�bonded�phases:�SB-C18,�SB-C8,�SB-Phenyl,�SB-CN,�and�SB-C3.�For�polaranalytes,�try�Bonus-RP,�SB-Aq�or�the�Polaris�family,�including�C18-A,�C8-A,�C18-Ether�and�Amide-C18�phases.

It�may�be�necessary�at�low�pH�to�improve�the�retention�of�acidic�compounds.�For�these�situations,�lower�the�pH�even�further,�down�to�pH�1-2,�and�use�StableBond�columns.�These�columns�provide�the�greatest�stability�at�very�low�pH�and�provide�many�selectivity�options�for�achieving�the�highest�resolution�separations.

LC Method Translator

Use�this�online�tool�to�quickly�factor�in�changes�to�column�length,�diameter,�flow�rate,and�more�–�and�to�calculate�method�adjustments.�This�is�particularly�useful�for�gradient�methods.

To�download,�go�to�www.agilent.com/chem/lcmethodtranslator

TiPS & TooLS



Choose Agilent ZORBAX Eclipse Plus or Poroshell 120 for method development at mid pH (pH 4-9)There�are�some�samples�that�may�not�be�resolved�at�low�pH�or�may�have�better�solubility�and�stability�at�mid�pH.�The�Eclipse�Plus�C18�and�Poroshell�120�EC-C18�columns�can�be�used�at�the�mid�pH�range�for�method�development.�The�Eclipse�Plus�column�is�stable�to�pH�9�so�it�is�equally�reliable�at�mid�pH.�These�double�endcapped�columns�have�two�key�advantages�–�good�peak�shape�at�low�and�mid�pH,�as�well�as�sufficient�bonded�phasedensity�to�protect�the�column�from�silica�degradation�from�pH�6-9.

At�mid�pH,�basic�compounds�(e.g.,�amines)�may�still�have�a�positive�charge�and�the�silanols�on�the�silica�surface�may�have�a�negative�charge.�Therefore�covering�as�many�silanols�as�possible�leads�to�the�best�peak�shape�at�mid�pH.�This�makes�the�Eclipse�Plus�C18�the�best�starting�choice�for�a�column�at�mid�pH.�Phosphate�buffer�is�usually�the�first�choice�for�mobile�phase�modifier�at�pH�7�because�its�buffer�range�is�pH�6.1-8.1.�A�second�choice�for�mid�pH�is�acetate�buffer�since�it�buffers�from�pH�3.8-5.8�and�its�volatility�makes�it�a�good�choice�for�LC/MS�compatibility.

Agilent�offers�a�full�line�of�pH�meters�and�electrodes.�Designed�for�chromatographers,�these�pH�meters�offer�intuitive�user�design�and�exceptional�ruggedness�for�your�lab.�Learn�more�atwww.agilent.com/chem/agilentpH

Choose Agilent ZORBAX Extend-C18 columns for method development at high pH (pH 9-12)At�low�or�mid�pH,�some�separations�of�basic�compounds�may�still�not�have�enough�retention�or�the�desired�selectivity.�For�these�samples,�high�pHseparations�may�be�appropriate.�Until�recently,�high�pH�separations�on�silica-based�columns�were�avoided�because�of�short�column�lifetimes,�due�todissolution�of�the�underlying�silica�gel.�Special�bonded�phases�such�as�the�ZORBAX�Extend-C18,�can�protect�the�silica�from�dissolution,�so�that�a�reasonable�column�lifetime�can�be�achieved�and�the�selectivity�advantages�of�high�pH�can�be�explored.

EaSy, RELiaBLE PH TESTing

The�mobile�phase�buffer�choices�at�high�pH�with�the�Extend-C18�column�are�organic�buffers�like�triethylamine�and�ammonium�hydroxide.�These�buffers�arebest�used�with�methanol�as�the�organic�modifier�to�extend�the�column�lifetime�at�high�pH.�This�is�another�good�option�to�consider�when�working�with�highpH�and�PLRP-S�columns,�which�are�made�from�a�polymeric�material.

222


Method development guidelines from Low to High pH

Low pH 3.0

START

Initial separation

STEP 1

ZoRB

aX E

clip

se P

lus–

1 co

lum

n fo

r pH

2-9

Poorly retained compounds

Poorly retained compounds

SAMPLE

ü ZORBAX�Eclipse�Plus�C18,�C8,�orPoroshell�120�EC-C18

ü pH�2.5�(2-3)�20-50�mM�bufferü T=30�°C�(ambient�to�60�°C)ü Adjust�%�ACN�for�0.5�<�k�<�20

Acids

ü ZORBAX�SB-C18�or�SB-C8ü pH�1-3�20-50�mM�bufferü T�=�30�°C�(ambient�to�90�°C)ü Adjust�%�ACN�for�0.5�<�k�<�20

Bases OR

OR

Band spacing problems















Bandspacing

problems

Bandspacing

problems

BASIC�COMPOUNDS�(Ion-Pairing)ü Use�MeOH�organic�modifier,�10�mM�hexanesulfonic�acid,�25-50�mM�pH�3�buffer

ü Adjust�%�MeOH�for�0.5�<�k�<�20

STEP 1c

Increase�or�decrease�%�of�organic�modifierby�5%�(v/v)

Increase�or�decrease�%�oforganic�modifier�by�5%�(v/v)

Increase�or�decrease�%�oforganic�modifier�by�5%�(v/v)



STEP 1d

STEP 1e

ü Change�organic�modifier�(ACN�or�THF)ü Adjust�for�0.5�<�k�<�20

ü Change�organic�modifier�(ACN�or�THF)ü Adjust�for�0.5�<�k�<�20

STEP 2

STEP 3ü Change�organic�modifier�(MeOH�or�THF)ü Adjust�%�organic�for�0.5�<�k�<�20ü Vary�column�temperature,�up�to�60�°C�forEclipse�up�to�80-90�°C�for�Stablebond

ü Restart�at�STEP�2

STEP 4ü Change�bonded-phase�functionality�to�EclipsePlus�Phenyl-Hexyl,�Bonus-RP,�Eclipse�XDB-CN,SB-CN,�SB-Aq


Mid pH 7.0

STEP 5

Poorly retained acidic compounds

STEP 5aACIDIC�COMPOUNDS�(Ion-Pairing)ü Use�MeOH�organic�modifier,�10�mMtetrabutylammonium�phosphate,�25-50�mMpH�7�buffer

ü Adjust�%�MeOH�for�0.5�<�k�<�20

STEP 5bVary�temperature�within�recommendedrange�for�bonded�phase

STEP 5c

STEP 5d

STEP 6

STEP 7ü Change�organic�modifier�(ACN�or�THF)ü Adjust�for�0.5�<�k�<�20ü Restart�at�STEP�6

STEP 8ü Change�bonded�phase�functionality�to�ZORBAXEclipse�Plus�Phenyl-Hexyl�or�Bonus-RP


High pH 9.0

STEP 9ü ZORBAX�Extend-C18ü pH�10.5�(9-11.5);�5-20�mM�ammonia�or�TEA,or�10-50�mM�organic�buffer,�or�borate�buffer

ü T�=�25�°C�(ambient�to�40�°C)ü Adjust�%�MeOH�for�0.5�<�k�<�20

STEP 10ü Change�organic�modifier�(ACN�or�THF)ü Adjust�for�0.5�<�k�<�20ü Vary�temperature�within�recommended�rangefor�bonded�phase

Try different HPLC modeContact agilent Technologies

[email protected]

pH 4.0

pH 6.0

pH 8.0

pH 10.0

pH 11.0

pH 12.0

STEP 1a

STEP 1b

ü ZORBAX�Eclipse�Plus�C18,�C8�or�Poroshell�120�EC-C18

ü pH�7�(6-9),�20-50�mM�bufferü T�=�30�°C�(ambient�to�40�°C)ü Adjust�%�MeOH�for�0.5�<�k�<�20



guard Columns

Guard�columns�can�help�extend�the�life�of�your�analytical�column.�Choosing�to�use�guard�columns�can�helpreduce�operating�expenses,�by�reducing�the�frequency�of�analytical�column�replacement.

The�guard�column�prevents�damage�caused�by�particulate�matter�and�strongly�adsorbed�material.�To�maintain�an�adequate�capacity�for�sample�impurities,�choose�a�guard�column�with�an�internal�diametersimilar�to�the�column�internal�diameter.�Ideally,�the�packing�of�the�guard�column�should�be�the�same�as�theanalytical�column�so�that�the�chromatography�of�the�analytical�column�is�not�altered.�

Judging�when�to�replace�a�guard�column�can�be�difficult.�As�a�rough�guide,�if�plate�number,�pressure�orresolution�change�by�more�than�10%,�the�guard�column�probably�needs�replacing.�You�will�need�to�make�a�judgment�call�on�how�often�to�replace�your�guard�columns�based�on�your�application�type.�It�is�alwayspreferable�to�change�the�guard�column�sooner�rather�than�later.

The�Value�of�Guard�Columns

Guard�columns�contribute�to�the�separation,�so�you�should�include�a�guard�column�in-line�during�method�development.

Agilent�UHPLC�guards�provide�protection�for�high-efficiency�Poroshell�120�and�ZORBAX�RRHD�and�RRHT�columns,�without�reducing�performance.�Part�numbers�for�all�guard�columns�are�incorporated�into�the�different�product�family�tables.

UHPLC�Guard,�1200�bar,�821725-903

224


Cartridge Selection guide

icon* Type of Cartridge Features BenefitsAgilent�HPLC�Cartridge Can�reverse�collets�in�the�end�fitting�to�add

guard�cartridgesInexpensiveExtends�column�lifetimePermits�rapid�column�changesCan�use�2,�3,�4�and�4.6�mm�cartridges

Cartridges�have�a�unique�filter�and�sieve�at�each�end

Helps�prevent�blockage

ZORBAX�Guard�Cartridge:Standalone�system

High�efficiency,�standalone,�low-dead-volume�cartridge

Seals�up�to�5000�psi�(340�bar)�or�3000�psi�with�a�PEEK�fitting

Polymeric�cartridge�designed�for�leak-tight�seals�against�metal�surfaces

No�gaskets�requiredMore�solvent-resistant�than�PEEK

Reusable�fittings Adapt�for�connections�to�1/16�in�LC�fittingsZORBAX�Rapid�Resolution�and�RapidResolution�HT�Cartridge�Columns:3.5�µm�and�1.8�µm�packings,�Standalone�system

For�high�throughput�LC/MS,�LC/MS/MS�and�combinatorial�separationsPacked�with�Eclipse�XDB�for�pH�use�from�2-9Packed�with�StableBond�for�low�pH�use

For�all�analyte�typesLow�bleed

Sold�individually�or�as�three-packsZORBAX�Semi-Preparative�Guard�HPLC�Hardware�Kit:Standalone�system

Easy,�low-dead-volume�assembly Seals�up�to�2000�psi�(135�bar,�13.5�MPa)Tubing�(polyphenylene�sulfone)�designed�for�leak-tight�seals�against�metal�surfaces

No�gaskets�required

Reusable�fittings Adapt�for�connections�to�1/16�in�LC�fittingsZORBAX�and�Agilent�Prep�PreparativeCartridge�Column�and�Guard�HPLC�System:Standalone�and�integral�hardware�options

Easy,�low-dead-volume�assembly Extends�column�lifetimeReusable�fittings Permits�rapid�column�changesHardware�options�for�integral�and�external�guards Can�use�with�21.2�and�30�mm�id�columns

Polymeric�Analytical�Column�and�Guard�Cartridge

High�efficiency InexpensiveLow�dead�volume Rapid�cartridge�changesReusable�holder Extends�column�lifetime

ChromSep�Column�Hardware:Complete�systems�and�replacement�cartridges

Easy,�no-dead-volume�assembly Economical�formatNo�tools�requiredModular�flexibility

MetaGuard�Column�Hardware:Complete�systems�and�replacement�cartridges

Easy,�no-dead-volume�assembly Economical�formatNo�tools�requiredModular�flexibility

Agilent�Fast�Guards�for�UHPLC Requires�no�special�hardware�–�connects�right�to�the�analytical�column

Extends�column�lifetime�without�impacting�performance

Available�in�matching�phases�for�Poroshell�120,RRHD�and�RRHT�columns

*Look�for�these�icons�to�help�you�select�the�proper�guard�cartridges�and�columns.



Cartridge/guard Cartridge Systems Compatibility guide*

icon Column Type guard Cartridge Holderid(mm) Phases

Cartridge�column�cartridge�holder5021-1845

Guard�cartridge�(internal�system)�cartridge�holder5021-1845

2.03.04.04.6

LiChrospherNucleosilPurospherSuperspherZORBAX

Standard�fitting Column�guard�cartridge�(standalone)�cartridge�holder820999-901

2.13.04.6

ZORBAX

Rapid�Resolution�cartridge�holder820555-901

No�guard�cartridge�holder 4.6 ZORBAX

Semi-preparative�column Semi-prep�guard�cartridge�(standalone)�cartridge�holder840140-901

9.4 ZORBAX

(Continued)

226


PrepHT Guard�cartridge820444-901

21.2 ZORBAXAgilent�Prep

Analytical Guard�cartridge�holder�(PL1310-0016)�and�PLRP-Sguard�cartridges,�2/pk�(PL1612-1801)

3.0 PLRP-S

Single�replacement�column No�guard�cartridge�holder 1.02.04.6

PursuitPursuit�XRsPolaris�phases

Cartridge/guard Cartridge Systems Compatibility guide*

icon Column Type guard Cartridge Holderid(mm) Phases

Fast�Guards�for�UHPLC:�Single�replacement�guard�column

No�guard�cartridge�holder 2.13.04.6

Poroshell�120:EC-C18EC-C8SB-C18Phenyl-HexylSub-2�µm:Eclipse�Plus�C18Eclipse�XDB-C18SB-C18SB-C8

*Standalone�guard�cartridges�fit�all�cartridge�and�standard�fitting�columns�available�from�Agilent.�All�columns�without�icons�are�standard�fitting�columns.

nEw!



Fast Columns for Reversed-Phase HPLC/UHPLCThe�past�decade�has�seen�a�steady�increase�in�the�efficiency�and�speed�of�chromatography,�starting�withsmaller�particle�sizes,�that�enable�higher�resolution,�and�continuing�with�new�technological�advances�inparticle�design�–�superficially�porous�particles�–�that�enable�these�same�resolution�enhancements�withlower�backpressure.

Designed�especially�for�high-productivity�analysis�(Fast�LC),�Agilent�ZORBAX�and�Poroshell�columns�are�the�best�first�choice�for�any�analysis,�because�they�give�you:

• The�productivity�you�need�to�stay�ahead�of�your�competition:�technological�advances�like�sub-2�µmparticles�and�superficially�porous�Poroshell�120�columns�deliver�increased�speed�and�resolution.

• Flexibility�and�method�scalability�from�lab�to�lab�and�around�the�world�–�for�small�molecule�andbiomolecule�analyses.

• Unbeatable�chromatographic�performance:�ZORBAX�silica�–�the�base�silica�used�for�all�ZORBAX�and�Poroshell�120�columns�–�is�ultra-pure,�very�strong,�and�highly�uniform�for�ultimate�reliability.

• The�broadest�range�of�phases�and�column�configurations�to�suit�your�specific�application�needs.

Recommendations for Fast LC Columns

your Lab Situation agilent Recommends RationaleYou’re�using�both�UHPLC�(1000+�bar)�and�HPLC�instruments�(e.g.�Agilent�1290�Infinity�LC�and�1260�Infinity�LC�–�600�bar)

1.�Poroshell�120 Poroshell�120�is�an�easy�column�to�use�on�both�instrument�types.�ZORBAX�RRHD�will�help�you�optimize�the�capabilities�of�the�1290�Infinity�LC�for�UHPLC.

2.�ZORBAX�RRHD�1.8�µm

Only�400-600�bar�HPLCs�–�Agilent�1200s,�Agilent�1100s�(400�bar)�as�well�as�the�1220�Infinity�LC�or�1260�Infinity�LC�(600�bar)

1.�Poroshell�120 With�Poroshell�120,�you�can�enhance�the�performance�of�older�400-bar�instruments,�and�also�get�even�better�performance�fromnewer�600�bar�UHPLC�instruments.�For�established�methods�that�you�can’t�transfer,�the�ZORBAX�Eclipse�Plus�column�will�provideexceptional�peak�shape�and�performance.

2.�ZORBAX�Eclipse�Plus�3.5�µm�and�5�µm

A�mix�of�UHPLC�instruments�(Agilent�1290�Infinity�LC,�other�1000+�bar�instruments)�and�some�HPLC�instruments�(e.g.�1200�LC)

1.�ZORBAX�RRHD�1.8�µm ZORBAX�RRHD�can�deliver�optimum�performance�on�all�theseinstruments.�Poroshell�120�can�be�used�on�the�600�bar�instruments�to�optimize�their�performance.

2.�Poroshell�120

TiPS & TooLS

Agilent�CrossLab�offers�a�range�of�PEEK�capillaries�and�tubing.�Used�in�combination�with�the�right�fittings,they�provide�an�inert�surface�for�the�Fast�LC�of�sensitive�biomolecules. Turn�to�page�130.

228


Solid�core,�1.7�µm�diameter

Porous�shell,�0.5�µm�thick

• High�efficiency�and�high�resolution,�with�up�to�50%�less�backpressure�than�sub-2�µm�columns• 2�µm�frit,�for�rugged�performance�with�dirty�samples• Compatible�with�400�bar�and�600�bar�LCs,�as�well�as�UHPLC�instruments• An�expanding�family�of�bonded�phases�to�align�with�the�ZORBAX�Family,�for�reliable�scalability• Excellent�selectivity�and�peak�shapes• Designed�for�exceptional�reproducibilityAgilent�Poroshell�120�columns�are�a�2.7�µm�particle�with�a�1.7�µm�solid�core�and�0.5�µm�porous�outer�layer.This�small�particle�size�provides�high�efficiency,�similar�to�sub-2�µm�columns,�but�with�40-50%�less�pressure.These�high�efficiency,�high�resolution�columns�can�be�used�on�any�type�of�LC.�The�porous�outer�layer�andsolid�core�limit�diffusion�distance�and�improve�separation�speed�while�the�narrow�particle�size�distributionimproves�efficiency�and�resolution.�The�columns�can�support�high�pressure�and�multiple�columns�can�beused�for�the�highest�resolution�and�efficiency�possible.�The�same�principles�are�used�in�Poroshell�300columns,�ideal�for�fast,�high�resolution�separations�of�biomolecules.��

Poroshell 120

TiPS & TooLS

Column Specifications

Bonded Phase Pore Size Temp Limits pH Range Endcapped Carbon Load Surface areaEC-C18 120Å 60�°C 2.0-8.0 Double 10% 130�m2/gEC-C8 120Å 60�°C 2.0-8.0 Double 5% 130�m2/gPhenyl-Hexyl 120Å 60�°C 2.0-8.0 Double 9% 130�m2/gSB-C18 120Å 90�°C 1.0-8.0 No 8% 130�m2/gSB-C8 120Å 80�°C 1.0-8.0 No 5.5% 130�m2/gSB-Aq 120Å 80�°C 1.0-8.0 No Proprietary 130�m2/gBonus-RP 120Å 60�°C 2.0-9.0 Triple 9.5% 130�m2/gEC-CN 120Å 60�°C 2.0-8.0 Double 3.5% 130�m2/gHILIC 120Å 60�°C 0.0-8.0 No N/A 130�m2/g

Specifications�represent�typical�values�only

Watch�the�Poroshell�120�Method�Transfer�Video�to�learn�how�easy�it�is�to�transfer�existingmethods�to�Poroshell�120�at�www.agilent.com/chem/poroshell120video



Poroshell 120(Maximum pressure: 600 bar)

Hardware description Size (mm)

ParticleSize(µm)

EC-C18uSP L1

EC-C8uSP L7

Phenyl-HexyluSP L11

SB-C18uSP L1

SB-C8uSP L7 SB-aq

Bonus-RPuSP L60

Analytical 4.6�x�150 2.7 693975-902 693975-906 693975-912 683975-902 683975-906 683975-914 693968-901Analytical 4.6�x�100 2.7 695975-902 695975-906 695975-912 685975-902 685975-906 685975-914 695968-901Analytical 4.6�x�75 2.7 697975-902 697975-906 687975-902Analytical 4.6�x�50 2.7 699975-902 699975-906 699975-912 689975-902 689975-906 689975-914 699968-901Analytical 4.6�x�30 2.7 691975-902 691975-906 681975-902UHPLC�Guard,600�bar,�3/pk

4.6�x�5 2.7 820750-911 820750-913 820750-914 820750-912

Solvent�Saver 3.0�x�150 2.7 693975-302 693975-306 693975-312 683975-302 683975-306 683975-314 693968-301Solvent�Saver 3.0�x�100 2.7 695975-302 695975-306 695975-312 685975-302 685975-306 685975-314 695968-301Solvent�Saver 3.0�x�75 2.7 697975-302 697975-306 687975-302Solvent�Saver 3.0�x�50 2.7 699975-302 699975-306 699975-312 689975-302 689975-306 689975-314 699968-301Solvent�Saver 3.0�x�30 2.7 691975-302 691975-306 681975-302UHPLC�Guard,600�bar,�3/pk

3.0�x�5 2.7 823750-911 823750-913 823750-914 823750-912

Narrow�Bore 2.1�x�150 2.7 693775-902 693775-906 693775-912 683775-902 683775-906 683775-914 693768-901Narrow�Bore 2.1�x�100 2.7 695775-902 695775-906 695775-912 685775-902 685775-906 685775-914 695768-901Narrow�Bore 2.1�x�75 2.7 697775-902 697775-906 687775-902Narrow�Bore 2.1�x�50 2.7 699775-902 699775-906 699775-912 689775-902 689775-906 689775-914 699768-901Narrow�Bore 2.1�x�30 2.7 691775-902 691775-906 681775-902UHPLC�Guard,600�bar,�3/pk

2.1�x�5 2.7 821725-911 821725-913 821725-914 821725-912

Poroshell�120�Columns

230


Time (min)

Time (min) EP_Poro120

0 2 4 6 8 10

0 2 4 6 8 10

A

B

10

45

67

8

9

10

12

3

12

34

5

67

8

9

Environmental phenols on Poroshell 120Column a: Poroshell 120 EC-C18

695975-9024.6 x 100 mm, 2.7 µm

Column B: Eclipse Plus C18959964-9024.6 x 100 mm, 1.8 µm

Gradient: A:�Water�0.1%�formic�acidB:�Acetonitrile�0.1%�formic�acid2�mL/minInitial:�8%�B10�min:�30%�B

Detector: 275�nm,�2�mm�flow�cell

Injection: 10�µL

Agilent�1200�SL�40�°C

No�pulse�damper

No�mixer�3�µL�heater

Poroshell�120�provides�sub-2�µm�like�efficiency�at�lower�pressure.

2.5 5 7.5 10

0.64

6 0

.826

1.14

8 1

.518

2.01

6 2

.223

2.81

6

4.13

2

6.27

3

9.75

3

2.5 5 7.5 10 12.5

0.64

9 0

.865

1.27

5 1

.756

2.41

8 2

.705

3.49

4

5.28

1

8.218

13.0

41 min

A

B

1. Hydroquinone2. Resorcinol3. Catechol4. 4-Nitrophenol5. p-cresol

6. o-cresol7. 2-Nitrophenol8. 2,3�Dimethyl�phenol9. 2,5�Dimethyl�phenol10. 1-Naphthol

P = 332 bar

P = 510 bar

n = 25053, Press = 182 bar

n = 27295, Press = 386 bar

uHPLC efficiency at HPLC pressuresColumn a: Poroshell 120 EC-C18

695975-3023.0 x 100 mm, 2.7 µm

Column B: Eclipse Plus C18959964-3023.0 x 100 mm, 1.8 µm

Mobile�Phase: 60%�Acetonitrile:40%�water

Flow�Rate: 0.58�mL/min

Temperature: 26�°C

Injection�Volume:� 4�µL

Detector: DAD�Sig�=�254,4�nmRef�=�360,100�nm

Sample: RRLC�checkout�sample�(P/N�5188-6529)�spiked�w/50�µL�2�mg/mL�thiourea�in�water/acetonitrile�(65:35)

For�this�sample�of�neutral�alkylphenones,�the�Poroshell�120�column�delivered�>90%�of�the�efficiency�attained�by�the�1.8�µm�column.�Also�note�that�the�pressure�on�thePoroshell�120�column�is�about�50%�of�the�pressure�on�the�1.8�µm�column.



0 5 min

Importantly,�the�flow�rate�was�kept�to�2.5�mL/min,reducing�the�amount�of�mobile�phase�consumed�peranalysis�to�about�15�mL.

Agilent�Poroshell�120�gives�high�efficiency,�highresolution�separations�quickly�at�HPLC�pressures.

1. Hydroquinone2. Resourcinol3. Catechol4. Phenol5. 4-Nitrophenol6. p-cresol7. o-cresol8. 2-Nitrophenol9. 3,4�di�methyl�phenol10. 2,3�di�methyl�phenol11. 2,5�di�methyl�phenol12. 1-napthol

HPLC separation of 12 phenols performed in just 5 minutes – and under 400 bar – using an agilent Poroshell 120 EC-C18 columnColumn: Poroshell 120 EC-C18

699975-9024.6 x 50 mm, 2.7 µm

Mobile�Phase: Solvent�A:�Water�with�0.1%�formic�acidSolvent�B:�Acetonitrile

Gradient: 5%�B�in�0.8�min60%�B�in�6.8�min1200�SL�controlled�temperature�at�25�°C�2�mm�flow�cell


2.5 mL/min, 274 bar

20

40

60

80

100

2 4 6 8 10 12

0

mAU

min

12 phenols analyzed using a longer (4.6 x 100 mm)agilent Poroshell 120 EC-C18 columnColumn: Poroshell 120 EC-C18

695975-9024.6 x 100 mm, 2.7 µm

Mobile�Phase: Solvent�A:�Water�with�0.1%�formic�acidSolvent�B:�Acetonitrile

Gradient: 5%�B�in�2�min60%�B�in�17�min1200�RRLC�SL�controlled�temperature�at�25�°C�2�mm�flow�cell


1. Hydroquinone2. Resourcinol3. Catechol4. Phenol5. 4-Nitrophenol6. p-cresol7. o-cresol8. 2-Nitrophenol9. 3,4�di�methyl�phenol10. 2,3�di�methyl�phenol11. 2,5�di�methyl�phenol12. 1-napthol

By�reducing�the�flow�rate�to�2.0�mL/min,�thepressure�was�kept�to�less�than�400�bar�improvingthe�separation�of�a�late-eluting�peak�pair(highlighted)�with�only�a�minor�increase�in�analysistime.�This�separation�can�be�achieved�using�HPLC�or,if�a�higher�flow�rate�is�desired,�a�UHPLC.

2.0 mL/min, 394 bar

232


2 4 6 0

100200300

2 4 0

100

200

300

mAU

mAU

mAU

2 4 0

100

200

min

1. Saccharin2. Caffeine3. P-hydroxybenzoic�acid4. Aspartame5. Dehydroacetic�acid6. Benzoic�acid

Poroshell 120 EC-C18 for fast uHPLC separationsColumn: Poroshell 120 EC-C18

695975-3023.0 x 100 mm, 2.7 µm

Mobile�Phase: 65%�A:�0.2%�Formic�acid35%�B:�MethanolIsocratic

Flow�Rate: Varies


Detector: Sig�=�220,�4�nm,�Ref�=�Off

This�example�shows�a�fast�separation�using�a�mobilephase�that�generates�higher�pressures.�In�the�topchromatogram,�a�3.0�mm�id�column�was�used,�with�a�flow�rate�of�0.5�mL/min�and�a�pressure�below�400�bar�–�making�this�a�typical�LC�separation.

Although�the�top�separation�was�fast�(just�under�6�minutes),�the�middle�and�bottom�chromatograms�show�that�you�can�reduce�run�times�to�under�3�minutesby�increasing�the�flow�rate.�These�faster�analyses�willtake�your�pressure�to�400-560�bar;�look�to�the�Agilent1200�Infinity�Series�flexible�upgrade�options�to�help�you�take�advantage�of�UHPLC�capabilities.

More�viscous�solvents�like�methanol�can�be�used�at�HPLC�or�UHPLC�pressures.

Flow Rate: 1.0 mL/min, P: 559 bar



TiPS & TooLS

For�a�full�listing�of�our�LC�capillary�portfolio,�turn�to�pages�16-46.



ZoRBaX Rapid Resolution High definition (RRHd) 1.8 µm

ZORBAX�Rapid�Resolution�High�Definition�(RRHD)�columns�are�an�expansion�of�the�ZORBAX�1.8�µm�particlecolumn�line.�The�new�RRHD�columns�use�improved�packing�processes�to�achieve�stability�up�to�1200�barfor�use�with�the�Agilent�1290�Infinity�LC�or�other�UHPLC�instruments.�RRHD�1.8�µm�columns�are�available�in�50,�100�and�150�mm�lengths�for�fast�or�high�resolution�–�truly�high�definition�–�separations�of�your�mostcomplex�samples.

• High�pressure�(1200�bar)�columns�for�optimum�results�with�the�1290�Infinity�LC�or�other�UHPLC�instruments�

• 1.8�µm�particles�deliver�maximum�resolution�for�the�most�defined�separations�• Available�in�12�ZORBAX�phases,�including�Eclipse�Plus�C18�for�superior�peak�shape,�ZORBAX�StableBond�C18�for�low�pH�stability,�Bonus-RP,�Eclipse�PAH,�Eclipse�Plus�Phenyl-Hexyl�and�Extend-C18

• Also�available�in�HILIC�Plus• Achieve�the�same�selectivity�on�3.5�and�5�µm�ZORBAX�columns�with�the�same�bonded�phase�forcompatibility�with�any�LC

ZoRBaX RRHd Column Specifications

Bonded Phase Pore Size Surface area pH Range Endcapped Temp LimitZORBAX�Eclipse�Plus�C18 95Å 160�m2/g 2.0-9.0 Double 60�°CZORBAX�Eclipse�Plus�C8 95Å 160�m2/g 2.0-9.0 Double 60�°CZORBAX�Eclipse�Plus�Phenyl-Hexyl 95Å 160�m2/g 2.0-9.0 Double 60�°CZORBAX�Eclipse�XDB-C18 80Å 180�m2/g 2.0-9.0 Double 60�°CZORBAX�Extend-C18 80Å 180�m2/g 2.0-11.5** Double 60�°CZORBAX�Bonus�RP 80Å 180�m2/g 2.0-9.0 Triple 60�°CZORBAX�StableBond�SB-C18 80Å 180�m2/g 1.0-8.0* No 80�°CZORBAX�StableBond�SB-C8 80Å 180�m2/g 1.0-8.0* No 80�°CZORBAX�StableBond�SB-Phenyl 80Å 180�m2/g 1.0-8.0* No 80�°CZORBAX�StableBond�SB-CN 80Å 180�m2/g 1.0-8.0* No 80�°CZORBAX�StableBond�SB-Aq 80Å 180�m2/g 1.0-8.0* No 80�°CZORBAX�Eclipse�PAH 95Å 160�m2/g 2.0-8.0 No 60�°CZORBAX�HILIC�Plus 95Å 160�m2/g 0.0-8.0 No 60�°CZORBAX�StableBond�300SB-C8 300Å 45�m2/g 1.0-8.0* No 80�°CZORBAX�StableBond�300SB-C18 300Å 45�m2/g 1.0-8.0* No 80�°CZORBAX�StableBond�300SB-C3 300Å 45�m2/g 1.0-8.0* No 80�°CZORBAX�300-Diphenyl 300Å 45�m2/g 1.0-8.0* No 80�°C

*�StableBond�columns�are�designed�for�optimal�use�at�low�pH.�At�pH�>6,�highest�column�stability�for�all�silica�based�columnsis�obtained�by�operating�at�temperatures�<40�°C�and�using�lower�buffer�concentrations�–�10-20�mM�or�organic�buffers.300SB-C18�may�be�used�up�to�90�°C.�For�pH�6-8,�select�the�Eclipse�Plus�C18�column.

**�Temperature�limits�are�60�°C�up�to�pH�8,�40�°C�from�pH�8-11.5.ZORBAX�Rapid�Resolution�High�Definition�(RRHD)

1.8�µm�Columns

234


min0

mAU

050

100150200

2 4 6 8 10 12 14 16 18

A

min0

mAU

050

100150200

2 4 6 8 10 12 14 16 18

B

min0

mAU

050

100150200

2 4 6 8 10 12 14 16 18

C

Rs: 2.40

Rs: 1.37

Rs: 0

150 mm

4 62

100 mm

42

42

50 mm

Separation of licorice root on RRHd columnsColumn a: ZoRBaX RRHd SB-C18

857700-9022.1 x 50 mm, 1.8 µm

Column B: 858700-9022.1 x 100 mm, 1.8 µm

Column C: 859700-9022.1 x 150 mm, 1.8 µm

Mobile�Phase: 10-100%�B/30�minA:�0.1%�Formic�acid�(fa)�B:�Acetonitrile�with�0.1%�fa

Flow�Rate: F�=�0.4�mL/min

Gradient: 30�minute�gradient�on�each�length

Temperature: Ambient

Detector: 280�nm�UV

Instrument:� 1290�Infinity�LC

7 peaks

8 peaks

9 peaks



×107

0

0.5

1

1.5

2 1

0.1 0.2 0.3 0.4 0.5 0.6 0.7 0.8 0.9 1 1.1 1.2 1.3 1.4 1.5 1.6 1.7 1.8 1.9 2

× 107

0

0.2

0.4

0.6

0.8

1

1.006

1

0.1 0.2 0.3 0.4 0.5 0.6 0.7 0.8 0.9 1

1.873

Average PW1/2 = 0.025

A

B

nc = 43

Average PW1/2 = 0.0092nc = 39

1. 2-methyl-4-isothiazolin-3-one2. 5-chloro-2-methyl-4-isothiazolin-3-one3. Carbendazim4. Benzisothiiazol-3(2H)-one5. 2-phenoxyethanol6. Methylparaben

min

RRHDSub1m

0 .05 .1 .15 .2 .25 .3 .35 .4 .45

mAU

0

100

200

300

400

500

1

2

3

45

6 0.5 min

Sub 1 minute separations with RRHd columnsColumn: ZoRBaX RRHd SB-C18

857700-9022.1 x 50 mm, 1.8 µm

Gradient: H2O�(0.05%�trifluoroacetic�acid)/10-40%�ACN/1�min�


Injection�Volume:� 0.5�µL�x�100�ppm�each

Detector:� UV,�275�nm

Data�Rate:� 160�Hz

6�compound�biocide�mix�in�0.5�min

F�=�2.0�mL/minP�=�975�bar

new levels of sensitivity and resolutionColumn a: ZoRBaX RRHd Eclipse Plus C18

959758-3023.0 x 100 mm, 1.8 µm

Column B: ZoRBaX RRHd Eclipse Plus C18959757-3023.0 x 50 mm, 1.8 µm

Ion�Source: 360�°C,�12�L/min.�50�psi,�3500�V.

Mobile�Phase: A:�0.2%�Formic�acid�in�waterB:�ACN

Temperature: Ambient,�no�temperature�control(approx�24�°C)

Detector: Agilent�1290�Infinity�LC�with�6410�MS/MS

Sample: 20�µL�(10�µL�for�50�mm�column)�of�1�µg/mL�standard

Compounds�(in�elution�order)�with�identifying�mass:1. Acetaminophen,�m/z�1092. Caffeine,�m/z�1943. 2-acetamidophenol,�m/z�1094. Acetanilide,�m/z�1355. Acetylsalicylic�acid,�m/z�1206. Phenacetin,�m/z�1797. Salicylic�acid,�m/z�1208. Sulindac,�m/z�3569. Piroxicam,�m/z�33210. Tolmetin,�m/z�25711. Ketoprofen,�m/z�25412. Diflunisal,�m/z�33213. Diclofenac,�m/z�23514. Celecoxib,�m/z�35115. Ibuprofen,�m/z�160

Counts�versus�Acquisition�time�(min)

Counts�versus�Acquisition�time�(min)

By�transferring�your�method�to�an�Agilent�RRHD�column,�you�can�enhance�resolution�for�difficult�analyses�–�allowing�you�tosave�time�by�using�shorter�columns�without�compromising�performance.

The�RRHD�column�saves�analytical�time�without�sacrificing�performance.

236


TiPS & TooLS

Selectivity comparison: C18 columnsColumn a: ZoRBaX RRHd Eclipse Plus C18

959758-9022.1 x 100 mm, 1.8 µm

Column B: ZoRBaX RRHd Eclipse XdB-C18981758-9022.1 x 100 mm, 1.8 µm

Column C: ZoRBaX RRHd Extend-C18758700-9022.1 x 100 mm, 1.8 µm

Column d: ZoRBaX RRHd SB-C18858700-9022.1 x 100 mm, 1.8 µm

Mobile�Phase: A:�0.1%�HCOOH�in�H2O�(30%)B:�0.1%�HCOOH�in�CH3CN�(70%)

Flow�Rate: 1�mL/min,�isocratic


Sample: 1�µL

MS2�Scan: 290-390,�ESI�positive�mode,�scan�time:�500,�fragmentor:�135�V;�drying�gas:�12�L/min,�325�°C;�nebulizer�pressure:�35�psig;�capillary�voltage:�3000

Selectivity�differences�are�due�to�subtle,�yet�importantvariations,�such�as�bonding�type,�endcapping,�or�the�amountand�type�of�silanols�on�the�silica.�Other�factors�that�influenceselectivity�include�mobile�phase�composition,�temperature,and�pH.�(Note�that�these�factors�are�identical�in�thefollowing�example.)

Here�we�compared�the�selectivity�of�four�Agilent�ZORBAX�RRHD�C18�columns�using�an�endocannabinoidanalysis�method.

×102

00.10.20.30.40.50.60.70.80.9

1

0.2 0.4 0.6 0.8 1 1.2 1.4 1.6 1.8 2 2.2 2.4 2.6 2.8 3 3.2 3.4

PEA

OEA

AEA

2-AG *

PEA

OEA

AEA

2-AG *

PEA

OEA

AEA

2-AG *

PEA

OEA

AEA

2-AG *

×102

00.10.20.30.40.50.60.70.80.9

1

0.2 0.4 0.6 0.8 1 1.2 1.4 1.6 1.8 2 2.2 2.4 2.6 2.8 3 3.2 3.4

×102

00.10.20.30.40.50.60.70.80.9

1

0.2 0.4 0.6 0.8 1 1.2 1.4 1.6 1.8 2 2.2 2.4 2.6 2.8 3 3.2 3.4

×102

00.10.20.30.40.50.60.70.80.9

1

0.2 0.4 0.6 0.8 1 1.2 1.4 1.6 1.8 2 2.2 2.4 2.6 2.8 3 3.2 3.4

1. Anadamine�(AEA),�m/z�3482. Palmitoylethanolamide�(PEA),�m/z�PEA3. 2-arachinoylglycerol�(2-AG),�m/z�379*4. Oleoylethanolamide�(OEA),�m/z�326

*A�fifth�peak�with�a�mass�of�379�was�also�detected.�This�impurity�is�believed�to�be�1,3�arachidonolyglycerol,�a�rearrangement�of�2-AG.

Counts�(%)�vs.�Acquisition�Time�(min)




a

B

C

d

For�full�details,�see�Agilent�publication�5990-7166EN,�www.agilent.com/chem/library



×102

00.10.20.30.40.50.60.70.80.91.0

1 2 3 4 5 6 7 8 9 10 11 12 13 14

1 2 3 4 5 6 7 8 9 10 11 12 13 14

1 2 3 4 5 6 7 8 9 10 11 12 13 14

×102

00.10.20.30.40.50.60.70.80.91.0

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15

15

15

15

×102

00.10.20.30.40.50.60.70.80.91.0

×102

00.10.20.30.40.50.60.70.80.91.0

Counts�(%)�versus�Acquisition�time�(min)

TiPS & TooLS

For�full�details,�see�Agilent�publication�5990-8470EN,�www.agilent.com/chem/library

Selectivity comparison: Phenyl and other columnsColumn a: ZoRBaX RRHd Eclipse Plus C18

959758-9022.1 x 100 mm, 1.8 µm

Column B: ZoRBaX RRHd Eclipse Plus Phenyl-Hexyl 959758-9122.1 x 100 mm, 1.8 µm

Column C: ZoRBaX RRHd SB-aq858700-9142.1 x 100 mm, 1.8 µm

Column d: ZoRBaX RRHd SB-Phenyl858700-9122.1 x 100 mm, 1.8 µm

Mobile�Phase: A:�5%�HCOOH�in�H2OB:�CH3CN


Gradient: 10-50%�B�in�15�min


MS2�Scan: ESI�+,�200-1000

Cyanidin,�m/z�286

Peonidin,�m/z�300

Delphinidin,�m/z�302

Petunidin,�m/z�316

Malvidin,�m/z�330

Extracted�ion�chromatograms�from�LC/MS�scan�data�of�blueberry�anthocyanins.

a

B

C

d

238


Rapid Resolution High definition (RRHd) Columns for High Pressure use (Maximum Pressure: 1200 bar)

Hardware description Size (mm)Particle Size

(µm)

EclipsePlus C18uSP L1


Eclipse PlusPhenyl-HexyluSP L11

EclipsePaHuSP L1

Solvent�Saver�RRHD,�1200�bar 3.0�x�150 1.8 959759-302 959759-306Solvent�Saver�RRHD,�1200�bar 3.0�x�100 1.8 959758-302 959758-306 959758-312 959758-318Solvent�Saver�RRHD,�1200�bar 3.0�x�50 1.8 959757-302 959757-306 959757-312 959757-318UHPLC�Guard,�1200�bar,�3/pk 3.0�x�5 1.8 823750-901Narrow�Bore�RRHD,�1200�bar 2.1�x�150 1.8 959759-902 959759-906 959759-912 959763-918Narrow�Bore�RRHD,�1200�bar 2.1�x�100 1.8 959758-902 959758-906 959758-912 959764-918Narrow�Bore�RRHD,�1200�bar 2.1�x�50 1.8 959757-902 959757-906 959757-912 959741-918UHPLC�Guard,�1200�bar,�3/pk 2.1�x�5 1.8 821725-901


Hardware description Size (mm)Particle Size

(µm)SB-C18uSP L1

SB-C8uSP L7

SB-CnuSP L10

SB-PhenyluSP L11 SB-aq

Solvent�Saver�RRHD,�1200�bar 3.0�x�150 1.8 859700-302 859700-306Solvent�Saver�RRHD,�1200�bar 3.0�x�100 1.8 858700-302 858700-306 858700-305 858700-905 858700-314Solvent�Saver�RRHD,�1200�bar 3.0�x�50 1.8 857700-302 857700-306 857700-305 857700-312 857700-314UHPLC�Guard,�1200�bar,�3/pk 3.0�x�5 1.8 823750-902 823750-904Narrow�Bore�RRHD,�1200�bar 2.1�x�150 1.8 859700-902 859700-906 859700-905 859700-912 859700-914Narrow�Bore�RRHD,�1200�bar 2.1�x�100 1.8 858700-902 858700-906 858700-905 858700-912 858700-914Narrow�Bore�RRHD,�1200�bar 2.1�x�50 1.8 857700-902 857700-906 857700-905 857700-912 857700-914UHPLC�Guard,�1200�bar,�3/pk 2.1�x�5 1.8 821725-902 821725-904


Hardware description Size (mm) Particle Size (µm)Extend-C18uSP L1

EclipseXdB-C18uSP L1

Bonus-RPuSP L60 HiLiC Plus

Solvent�Saver�RRHD,�1200�bar 3.0�x�150 1.8 759700-302 981759-302Solvent�Saver�RRHD,�1200�bar 3.0�x�100 1.8 758700-302 981758-302 959758-301Solvent�Saver�RRHD,�1200�bar 3.0�x�50 1.8 757700-302 981757-302 959757-301UHPLC�Guard,�1200�bar,�3/pk 3.0�x�5 1.8 823750-903Narrow�Bore�RRHD,�1200�bar 2.1�x�150 1.8 759700-902 981759-902 859768-901 959759-901Narrow�Bore�RRHD,�1200�bar 2.1�x�100 1.8 758700-902 981758-902 858768-901 959758-901Narrow�Bore�RRHD,�1200�bar 2.1�x�50 1.8 757700-902 981757-902 857768-901 959757-901UHPLC�Guard,�1200�bar,�3/pk 2.1�x�5 1.8 821725-903

ZORBAX�RRHD�columns�are�also�available�in�300Å�configurations�for�biomolecules.�Turn�to�page�364.ZORBAX�RRHD�300-HILIC�will�be�available�in�2013.



ZoRBaX Rapid Resolution High Throughput(RRHT) 1.8 µm• High�pressure�(600�bar)�columns�for�ultra�high�speed�or�maximum�resolution�analyses�with�Rapid�Resolution�HT�columns�packed�with�totally�porous,�1.8�µm�packings

• Carefully�engineered�particles�deliver�maximum�resolution�at�25%�less�pressure�than�other�sub-2�µm�materials

• Reduce�analysis�time�by�up�to�95%• Develop�HPLC�methods�more�quickly• Securely�transfer�conventional�methods�with�over�140�RRHT�column�choices�• Analyze�complex�samples�on�shorter�columns�faster�and�maximize�peak�capacity• Matching�selectivity�in�3.5,�5�and�7�µm�particle�sizes�for�complete�method�scalability• Short�(50�mm�long�and�less)�column�can�be�used�on�some�conventional�LCsAgilent�ZORBAX�Rapid�Resolution�HT�(1.8�µm)�columns�use�a�totally�porous,�1.8�µm�particle�to�providemaximum�resolution�in�fast,�ultra-fast�and�high�resolution�analyses.�You�can�reduce�analysis�time�by�up�to95%�in�comparison�to�250�mm�length�columns.�With�more�than�140�RRHT�column�choices,�including�thehigh�performance�ZORBAX�Eclipse�Plus�and�many�other�ZORBAX�column�choices�(Eclipse�XDB,�StableBond,Extend,�Bonus-RP),�methods�can�be�developed�quickly�or�securely�transferred�to�a�smaller�particle�sizecolumn�with�no�loss�in�resolution.�The�small�particle�size�provides�double�the�efficiency�of�a�3.5�µm�columnin�the�same�column�length,�providing�the�highest�efficiency�and�resolution�possible.�This�permits�the�analysisof�complex�samples�on�shorter�columns�with�the�highest�resolution�and�peak�capacity.�The�1.8�µm�RapidResolution�HT�columns�take�high-speed,�high-resolution�HPLC�to�a�new�level.��

The�600�bar�columns�can�be�used�with�the�Agilent1260�Infinity�LC�System�up�to�this�high�pressure�limit.�In�addition,�the�shorter�columns�can�be�used�on�many�other�LC's,�including�the�Agilent�1200�RapidResolution�LC�System.

ZORBAX�Rapid�Resolution�High�Throughput(RRHT)�1.8�µm�Columns

240


This�figure�shows�that�Rapid�Resolution�HT�columns�can�providedouble�the�efficiency�of�a�3.5�µm�column�in�the�same�column�length.�This�high�efficiency�can�be�used�for�very�high-resolution,�high�throughput�analyses.

Rapid Resolution HT (RRHT) provides doublethe efficiency of Rapid Resolution columnsColumn a: ZoRBaX Rapid Resolution SB-C18

835975-9024.6 x 50 mm, 3.5 µm

Column B: ZoRBaX RRHT SB-C18827975-9024.6 x 50 mm, 1.8 µm

Mobile�Phase: 25%�Water,�75%�MeOH



Detector: UV,�254�nm

LCRR002

Time (min)1.00.50.0

1

2

3

4

1

2

34

Time (min)

A B

10

1. Uracil2. Phenol3. 4-CI-Nitrobenzene4. Toluene

Plates (n)1. 3476

2. 4585

3. 5673

4. 6180

Plates (n)1. 6560

2. 8958

3. 11508

4. 12266

increase peak capacity with RRHT columnsColumn a: Eclipse RRHT XdB-C8

928700-9062.1 x 100 mm, 1.8 µm

Column B: Eclipse XdB-C18961753-9022.1 x 100 mm, 3.5 µm

Mobile�Phase: A:�H2OB:�ACN

Peak�capacity: A:�461B:�343


Gradient: 0.0�min�50%�B20.0�min�100%�B



Sample: Alkylphenones

LCRR004

1

11

Time (min)

A

B

0 2 4 6 8 12 14 16 1810

20406080

100120

mAU

0

1

11

Time (min)0 2 4 6 8 12 14 16 1810

20

40

60

80

100

mAU

0

1. Uracil2. C3-Alkylphenone3. C4-Alkylphenone4. C5-Alkylphenone5. C6-Alkylphenone6. C7-Alkylphenone7. C8-Alkylphenone8. C9-Alkylphenone9. C10-Alkylphenone10. C12-Alkylphenone11. C14-Alkylphenone



Reduce analysis time dramatically with RapidResolution HT columnsColumn a: Eclipse XdB-C18

990967-9024.6 x 250 mm, 5 µm

Column B: Eclipse XdB-C18963967-9024.6 x 150 mm, 3.5 µm

Column C: Eclipse XdB-C18966967-9024.6 x 75 mm, 3.5 µm

Column d: ZoRBaX Eclipse XdB-C18935967-9024.6 x 50 mm, 3.5 µm

Column E: Eclipse RRHT XdB-C18925975-9024.6 x 50 mm, 1.8 µm

Mobile�Phase: 73%�MeOH:27%�20�mMPhosphate�Buffer,�pH�7.0

Flow�Rate: 1�mL/min



LCRR003

1

432 5 76

1

432

576

1

432 576

1

4325 76

1

432

576

Time (min)

E

A

B

C

D

0 2 4 6 8 1210

This�figure�shows�the�dramatic�reduction�in�analysis�time�made�possible�by�using�Rapid�Resolution�HT�columns.�Chromatogram�A�shows�a�separation�that�takes�11.5�minutes�on�a�25�cm,�5�µm�column.�Rapid�Resolution�(3.5�µm)�columns,�shown�in�chromatogram�B�and�C,�reduce�analysis�time�substantially,�but�with�a�slight�compromise�in�resolution.�The�Rapid�Resolution�HT�column�reduces�analysis�time�to�2.2�minutes,�an�80%�reduction,�while�still�maintaining�baseline�resolution.

1. Uracil2. Naproxen3. Mefanamic�acid4. Butyl�paraben5. Propranolol6. Naphthalene7. Dipropyl�phthalate

LCRR005Injection Number

12000

Plates

10000

8000

6000

4000

499

718

853

988

1153

1305

1506

1641

1776

1911

2046

2181

2319

2508

2643

2778

2913

3085

3220

3468

3603

3738

3887

4054

4189

4324

4537

4756

4892

5033

52011

2000

0

Long lifetime of RRHT columns at elevatedtemperaturesColumn: ZoRBaX RRHT SB-C18

827700-9022.1 x 50 mm, 1.8 µm

Mobile�Phase: A:�60%�H2OB:�40%�ACN

Flow�Rate: 1�mL/min



Sample: QC�test�mix

242


TiPS & TooLS

The�LC�Rack�from�Agilent�can�help�you�reduce�capillary�lengths�and�minimize�extra-column�volume.It�also�protects�your�instrument�and�enables�you�to�switch�out�modules�as�needed.

Agilent�rack�for�LC�systems,�5001-3726

Comparison of efficiencies – Rapid Resolution High definition (RRHd)/RRHT (1.8 µm) and Rapid Resolution (3.5 µm) columns

Column Length (mm) Poroshell 120

ResolvingPower

n (3.5 µm)*

ResolvingPower

n (1.8 µm)High Resolution150 32,000 21,000 32,500100 21,000 14,000 24,00075 16,000 10,500 17,000**ultra Fast50 11,000 7,000 12,00030 5,500 4,200 6,00020 — — 3,50015 — 2,100 2,500Resolution�a N1/2

*5�µm�HPLC�columns�of�the�same�length�have�40%�fewer�plates�(N-value);�4.6�mm�id**Available�as�a�custom�columnData�is�based�on�4.6�mm�id�columns



Rapid Resolution HT Columns for High Pressure use (Maximum Pressure: 600 bar, 9000 psi)

Hardware descriptionSize(mm)

ParticleSize(µm)



Eclipse PlusPhenyl-HexyluSP L11

EclipsePaHuSP L1


EclipseXdB-C8uSP L7

Extend-C18uSP L1

Rapid�ResolutionHT,�600�bar

4.6�x�150 1.8 959994-902


4.6�x�100 1.8 959964-902 959964-906 959964-912 959964-918 928975-902 728975-902


4.6�x�75 1.8 959951-902


4.6�x�50 1.8 959941-902 959941-906 959941-912 959941-918 927975-902 927975-906 727975-902


4.6�x�30 1.8 959931-902 959931-906 959931-912 959931-918 924975-902 924975-906 724975-902


4.6�x�20 1.8 926975-902 926975-906 726975-902

UHPLC�Guard,600�bar,�3/pk

4.6�x�5 1.8 820750-901 820750-903

Solvent�Saver�HT,600�bar

3.0�x�100 1.8 959964-302 959964-306 959964-312 928975-302 728975-302


3.0�x�50 1.8 959941-302 959941-306 959941-312 927975-302 927975-306 727975-302


3.0�x�30 1.8 924975-302 924975-306 724975-302


3.0�x�20 1.8 926975-302 926975-306 726975-302


3.0�x�5 1.8 823750-901 823750-903

Narrow�BoreRRHT,�600�bar

2.1�x�150 1.8 959794-902


2.1�x�100 1.8 959764-902 959764-906 959764-912 959764-918 928700-902 928700-906 728700-902


2.1�x�50 1.8 959741-902 959741-906 959741-912 959741-918 927700-902 927700-906 727700-902


2.1�x�30 1.8 959731-902 959731-906 959731-912 924700-902 924700-906 724700-902


2.1�x�20 1.8 926700-902 926700-906 726700-902


2.1�x�5 1.8 821725-901 821725-903

244


Rapid Resolution HT Columns for High Pressure use (Maximum Pressure: 600 bar, 9000 psi)


ParticleSize(µm)

SB-C18uSP L1

SB-C8uSP L7

SB-PhenyluSP L11

SB-CnuSP L10 SB-aq

Rx-SiLuSP L3

Bonus-RPuSP L60


4.6�x�150 1.8 829975-902 829975-906 829975-912 829975-905 829975-914


4.6�x�100 1.8 828975-902 828975-906 828975-912 828975-905 828975-914 828975-901 828668-901


4.6�x�75 1.8 830975-906 830668-901


4.6�x�50 1.8 827975-902 827975-906 827975-912 827975-905 827975-914 827975-901 827668-901


4.6�x�30 1.8 824975-902 824975-906 824975-912 824975-905 824975-914


4.6�x�20 1.8 826975-902 826975-906


4.6�x�5 1.8 820750-902 820750-904


3.0�x�150 1.8 829975-302 829975-306 829975-312 829975-305


3.0�x�100 1.8 828975-302 828975-306 828975-312 828975-305 828975-314 828975-301 828668-301


3.0�x�50 1.8 827975-302 827975-306 827975-312 827975-305 827975-314 827975-301 827668-301


3.0�x�30 1.8 824975-302 824975-306 824975-305


3.0�x�20 1.8 826975-302 826975-306


3.0�x�5 1.8 823750-902 823750-904


2.1�x�150 1.8 820700-902 820700-906 820700-912 820700-905


2.1�x�100 1.8 828700-902 828700-906 828700-912 828700-905 828700-914 828700-901 828768-901


2.1�x�50 1.8 827700-902 827700-906 827700-912 827700-905 827700-914 827700-901 827768-901


2.1�x�30 1.8 824700-902 824700-906 824700-912 824700-905 824700-914


2.1�x�20 1.8 826700-902 826700-906


2.1�x�5 1.8 821725-902 821725-904



Rapid Resolution HT Columns and Cartridges (Maximum Pressure: 400 bar, 6000 psi)

Hardware description Size (mm)

ParticleSize(µm)


EclipseXdB-C8uSP L7

SB-C18uSP L1

SB-C8uSP L7

Extend-C18uSP L1

Rapid�Resolution�HT,�400�bar 4.6�x�50 1.8 922975-902 922975-906 922975-902 822975-906 722975-902Rapid�Resolution�HT,�3/pk,�400�bar 4.6�x�50 1.8 922975-932 922975-932Narrow�Bore�RRHT,�400�bar 2.1�x�50 1.8 922700-902 922700-902Narrow�Bore�RRHT,�3/pk,�400�bar 2.1�x�50 1.8 922700-932 922700-932

Rapid Resolution HT Cartridges (require hardware kit 820555-901)Rapid�Resolution�HT�Cartridge 4.6�x�50 1.8 925975-902 825975-902Rapid�Resolution�HT�Cartridge,�3/pk 4.6�x�50 1.8 925975-932 825975-932Rapid�Resolution�HT�Cartridge 2.1�x�50 1.8 925700-902 825700-902Rapid�Resolution�HT�Cartridge,�3/pk 2.1�x�50 1.8 925700-932 825700-932Rapid�Resolution�HT�Cartridge 4.6�x�30 1.8 923975-902 823975-902Rapid�Resolution�HT�Cartridge,�3/pk 4.6�x�30 1.8 923975-932 823975-932Rapid�Resolution�HT�Cartridge 2.1�x�30 1.8 923700-902 823700-902Rapid�Resolution�HT�Cartridge,�3/pk 2.1�x�30 1.8 923700-932 823700-932Rapid�Resolution�HT�Cartridge 4.6�x�15 1.8 921975-902 821975-902Rapid�Resolution�HT�Cartridge,�3/pk 4.6�x�15 1.8 921975-932 821975-932Rapid�Resolution�HT�Cartridge 2.1�x�15 1.8 921700-902 821700-902Rapid�Resolution�HT�Cartridge,�3/pk 2.1�x�15 1.8 921700-932 821700-932Hardware�Kit�for�RR�and�RRHT�Cartridges 820555-901 820555-901

246


agilent Fast guards for uHPLC• High�performance�guard�columns�for�Fast�LC�columns• Two�formats�–�one�for�Poroshell�120�columns,�stable�to�600�bar,�RRHD�columns,�1.8�µm�(stable�to�1200�bar),�and�RRHT�columns,�1.8�µm�(stable�to�600�bar)

Agilent�UHPLC�Guards�are�high�performance�guards�designed�by�Agilent�for�its�Fast�LC�columns�families.Agilent�UHPLC�Guards�use�easy-to-install�hardware�that�fits�directly�on�the�end�of�the�column;�no�extrahardware�is�needed.�They�are�sold�in�packages�of�three.

Agilent�UHPLC�Guards�extend�the�lifetime�of�analytical�columns�without�diminishing�performance.

Fast guards for uHPLCZoRBaX RRHd columns, 1.8 µm (1200 bar), and ZoRBaX RRHT columns, 1.8 µm (600 bar)


Particle Size (µm)


Eclipse XdB-C18uSP L1

SB-C18uSP L1

SB-C8uSP L7

UHPLC�Guard,�1200�bar,�3/pk 2.1�x�5 1.8 821725-901 821725-903 821725-902 821725-904UHPLC�Guard,�1200�bar,�3/pk 3.0�x�5 1.8 823750-901 823750-903 823750-902 823750-904UHPLC�Guard,�600�bar,�3/pk 4.6�x�5 1.8 820750-901 820750-903 820750-902 820750-904

Poroshell 120 columns, 2.7 µm (600 bar)


Particle Size (µm)

EC-C18uSP L1

EC-C8uSP L7

SB-C18uSP L1

Phenyl-HexyluSP L11

UHPLC�Guard,�600�bar,�3/pk 2.1�x�5 2.7 821725-911 821725-913 821725-912 821725-914UHPLC�Guard,�600�bar,�3/pk 3.0�x�5 2.7 823750-911 823750-913 823750-912 823750-914UHPLC�Guard,�600�bar,�3/pk 4.6�x�5 2.7 820750-911 820750-913 820750-912 820750-914

UHPLC�Guard,�1200�bar,�821725-903

Learn�about�Fast�Guards�for�UHPLC�–�an�easy�way�to�extend�the�life�of�your�analytical�Fast�LC�column�without�losing�performance.�www.agilent.com/chem/fastguardsvideo

TiPS & TooLS

247www.AgiLEnt.COM/CHEM/LC

COLUMnS fOR SMALL MOLECULE SEPARAtiOnS

Other Columns for Reversed-Phase Analytical HPLC

Whether you are using Fast LC or working with more conventional HPLC applications, Agilent’s LC familyoffers you a range of phases and selectivities to help you perfect your separation.

ZORBAX Rapid Resolution, 3.5 µm, configurations are an ideal choice for initial method development,providing increased sample throughput for any application when compared to 5 µm columns.

ZORBAX Solvent Saver 3.0 mm id column configurations provide 60% mobile phase reduction over 4.6 mm id columns.

ZORBAX Eclipse Plus HPLC columns are designed to reliably produce superior peak shapes for basiccompounds, and are available across all ZORBAX column configurations.

More than 13 additional ZORBAX phases including StableBond, Eclipse PAH, Eclipse XDB, ZORBAX Rx, Extend-C18, Bonus-Rx and Original ZORBAX columns – in total, more than 1400 configurations for reliable scalability and method transfer.

ZORBAX Method Development kits contain three columns for the price of two! Each as a differentbonded phase for optimizing selectivity.

ZORBAX Method Validation kits – choose as many columns as you need (or as few) to make methodvalidation easier and less expensive.

Pursuit, Pursuit XRs and Pursuit XRs Ultra columns provide alternate selectivities to the ZORBAX family.

Polaris Columns provide polar-modified phases for routine polar applications.

Other Columns for Reversed-Phase Analytical HPLC.

Achieve excellent peak shape and resolution every time –leveraging the industry’s broadest selection of reversed-phase columns

The ZORBAX Family of phases scales readily to Fast LC columns in the Rapid Resolution High Throughput(RRHT) and Rapid Resolution High Definition (RRHD) families and Poroshell 120 columns, see previoussection, page 227.

In this section, we’ll provide overviews of other key analytical columns from Agilent:

248


Agilent ZORBAX Eclipse Plus columns provide the ultimate in performance for silica-based columns. Peak shape is excellent for the most challenging basic compounds, improving efficiency and resolution withthese sample types. These results are achieved by improvements in the silica manufacturing and bondingtechnology, which is completely controlled by Agilent.

Because of their high level of performance, Eclipse Plus columns are the ideal first choice for methoddevelopment of all samples. If you need to achieve fast method development and superior productivity, thenchoose a column with high-resolution 1.8 µm particles. For standard methods, conventional 5 µm and RapidResolution 3.5 µm columns are your best choice. With all particle sizes, easy method transfer is possible.

With more rigorous QA and QC testing, column lot-to-lot reproducibility is also improved, resulting in long-term reliable results for all analyses.


Bonded PhasePoreSize

SurfaceArea

temp.Limits pH Range* Endcapped

CarbonLoad

ZORBAX Eclipse Plus C18 95Å 160 m2/g 60 °C 2.0-9.0 Double 9%ZORBAX Eclipse Plus C8 95Å 160 m2/g 60 °C 2.0-9.0 Double 7%ZORBAX Eclipse PAH 95Å 160 m2/g 60 °C 2.0-8.0 No 14%ZORBAX Eclipse Plus Phenyl-Hexyl

95Å 160 m2/g 60 °C 2.0-8.0 Double 9%

Specifications represent typical values only.*Column lifetime will be reduced significantly at pH >7 and temperature >40 °C. At pH 6-9, highest column stability for all silica based columns is obtained by operating at temperatures <40 °C and using lower buffer concentrations in range of 0.01-0.02 M, especially with phosphate and carbonate buffers.

tiPS & tOOLS

The EC-C18, EC-C8 and Phenyl-Hexylphases on Poroshell 120 are verysimilar to Eclipse Plus C18, Eclipse Plus C8 and Eclipse Plus Phenyl-Hexyl phases.

Turn to page 228.

• The ideal column for method development – excellent results for a wide range of compounds• High level of performance – peak shape, efficiency, resolution, and lifetime – with all sample types:

acids, bases and neutrals• Superior reproducibility with more rigorous QA/QC testing• Improved, patented silica manufacturing with start-to-finish product control• Available in 1.8, 3.5, and 5 µm particle sizes for all analytical, high resolution, and fast LC analyses

ZORBAX Eclipse Plus

ZORBAX Eclipse Plus Columns



LCEC001

1

2

Time (min)

Eclipse Plus C18

Ace 5 C18

SunFire C18

XBridge C18

Discovery HS C18

Luna C18 (2)

Gemini C18

XTerra MS C18

0 1.0 2.0 3.00.5 1.5 2.5 3.5

ZORBAX Eclipse Plus: Best peak shape in the industry without tailingColumn: Eclipse Plus C18

959996-9024.6 x 100 mm, 5 µm

Mobile Phase: A: 60% WaterB: 40% Acetonitrile

Flow Rate: 1.0 mL/min


Detector: UV, 254 nm

Sample: Pyridine, Phenol

1. Pyridine2. Phenol

A

B

Time (min)

LCEC003

0 2 4 6 8 10 12

N = 14000Tf = 1.25

N = 41000Tf = 1.13

N = 60000Tf = 1.00

N = 23000Tf = 1.01

65432

1

Time (min)0 2 4 6 8 10 12

65432

1

Peak shape and efficiency are better with ZORBAX Eclipse PlusColumn A: XBridge C18, 4.6 x 150 mm, 5 µmColumn B: Eclipse Plus C18

959993-9024.6 x 150 mm, 5 µm

Mobile Phase: A: 0.1% Formic acidB: 0.1% Formic acid in ACN


Gradient: 0.0 min 10% B15 min 30% B

Temperature: 40 °C


Sample: Sulfonamides

1. Sulfanilamide2. Sulfadiazine3. Sulfathiazole4. Sulfamerazine5. Sulfmethazine6. Sulfamethoxazole

min0 0.5 1 1.5 2

1

1

2

2

A

B

N: 6600Pw : 0.037 min.TF: 0.99 N: 6300

Pw : 0.061 min.TF: 0.98

N: 5000Pw : 0.019 min.TF: 1.09

N: 8800Pw : 0.014 min.TF: 1.20

N: 11600Pw : 0.047 min.TF: 1.06

N: 11800Pw : 0.093 min.TF: 1.02

min0 1 2 3 4

min0 1 2 3 4

A

B

2.2 min.

Eliminate tailing and maximize resolution with Eclipse Plus ColumnsColumn A: Eclipse Plus C18, 4.6 x 50 mm

Column B: Competitive C18, 4.6 x 50 mmMobile Phase: 65% ACN:35% 25 mM phosphate buffer (pH 7.4)

1. Nortriptyline2. Dipropylthalate

Tf = 1.20

Tf = 4.86

Superior peak shape and better selectivity with Eclipse Plus means more resolution,easier quantitation and better results in your separations.

Eclipse Plus C18, 4.6 x 50 mm

Competitive C18, 4.6 x 50 mm

Eclipse Plus C18 vs. C8Column A: Eclipse Plus C18

4.6 x 50 mm, 5 µmColumn B: Eclipse Plus C8

4.6 x 50 mm, 5 µmMobile Phase: Water: acetonitrile (30:70)


Temperature: 30 °C


Sample: Lip balm extract in ACN(melted at 100 °C, cooled and 0.45 µm filtered)

1. Oxybenzone2. Internal Std.3. Octylmethoxycinnamate

250


Less retention can save significant time – the C8 is a good choice here.

0 0.5 1 1.5 2 2.5 3 3.5 min

4

pH 2.73

2

1

pH 7.0

0 0.5 1 1.5 2 2.5 3 3.5 min

1

2

3

4

2 min.

Rapid analysis of an analgesic tablet, selectivity differences at pH 2 and pH 7Column: Eclipse Plus C8

959946-9064.6 x 50 mm, 5 µm

Gradient: 10-60% B/3 minpH 2.7: A: 0.1% Formic acid B: 0.1% fa in ACNpH 7.0: A: 20 mM Na phosphate B: ACN

Sample: generic Excedrin tablet

1. Acetaminophen2. Caffeine3. Acetylsalicylic acid4. Unknown

Both Eclipse Plus C18 and C8 can be used over a wide pH range to optimizeselectivity or analysis time.



00 1 2 3 4 5 6 7 8 9 min

Tf=1.04

Tf=1.00

00 1 2 3 4 5 6 7 8 9 min

3.789

A

B 5.777

Eclipse Plus C8 is less retentive than Eclipse Plus C18Column A: Eclipse Plus C8

959996-9064.6 x 100 mm, 5 µm

Column B: Eclipse Plus C18959996-9024.6 x 100 mm, 5 µm

Mobile Phase: 80% Methanol 8 mM (total) K2HPO4 pH 7



Sample: Amitriptyline 0.05 µg/µL (0.5 µL injection)

A C8 column is typically selected because it will retain less than a C18 column,reducing analysis time.

The Eclipse Plus C8 column shows the same behavior with excellent peak shapeon difficult basic compounds.

min

EP103

0 0.5

A

1 1.5 2 2.5

O

OCH3Tf = 1.00

OCH3

O N+ Cl-

min0 0.5 1 1.5 2 2.5

B

Tf = 1.06

fast and ultra-fast analysis of basic compoundson Eclipse PlusColumn A: Eclipse Plus C18

959941-9024.6 x 50 mm, 1.8 µm

Column B: Eclipse Plus C18959993-9024.6 x 150 mm, 5 µm

Mobile Phase: A: 50% 8 mM K2HPO4, pH 7B: 50% ACN




Sample: Berberine, 0.4 mg/mL, 2 µL

1. Berberine

ZORBAX Eclipse Plus Columns

Agilent HILIC Plus uses the same manufacturing processes as the Eclipse Plus family. See information about ZORBAX HILIC Plus on

252


(Continued)

ZORBAX Eclipse Plus

Hardware Description Size (mm)Particle Size

(µm)

EclipsePlus C18USP L1


Eclipse PlusPhenyl-HexylUSP L11

EclipsePAHUSP L1

Analytical 4.6 x 250 5 959990-902 959990-906 959990-912 959990-918Analytical 4.6 x 150 5 959993-902 959993-906 959993-912 959993-918Analytical 4.6 x 100 5 959996-902 959996-906 959996-912 959996-918Analytical 4.6 x 50 5 959946-902 959946-906Rapid Resolution 4.6 x 150 3.5 959963-902 959963-906 959963-912 959963-918Rapid Resolution 4.6 x 100 3.5 959961-902 959961-906 959961-912 959961-918Rapid Resolution 4.6 x 75 3.5 959933-902 959933-906 959933-912Rapid Resolution 4.6 x 50 3.5 959943-902 959943-906 959943-912 959943-918Rapid Resolution 4.6 x 30 3.5 959936-902 959936-906 959936-912Rapid Resolution HT, 600 bar 4.6 x 100 1.8 959964-902 959964-906 959964-912 959964-918Rapid Resolution HT, 600 bar 4.6 x 75 1.8 959951-902Rapid Resolution HT, 600 bar 4.6 x 50 1.8 959941-902 959941-906 959941-912 959941-918Rapid Resolution HT, 600 bar 4.6 x 30 1.8 959931-902 959931-906 959931-912 959931-918UHPLC Guard, 600 bar, 3/pk 4.6 x 5 1.8 820750-901Solvent Saver 3.0 x 250 5 959990-318Solvent Saver 3.0 x 150 5 959993-302 959993-306Solvent Saver Plus 3.0 x 150 3.5 959963-302 959963-306 959963-312Solvent Saver Plus 3.0 x 100 3.5 959961-302 959961-306 959961-312Solvent Saver RRHD, 1200 bar 3.0 x 150 1.8 959759-302 959759-306Solvent Saver RRHD, 1200 bar 3.0 x 100 1.8 959758-302 959758-306Solvent Saver RRHD, 1200 bar 3.0 x 50 1.8 959757-302 959757-306Solvent Saver HT, 600 bar 3.0 x 100 1.8 959964-302 959964-306 959964-312Solvent Saver HT, 600 bar 3.0 x 50 1.8 959941-302 959941-306 959941-312

page 324.



UHPLC Guard, 1200 bar, 3/pk 3.0 x 5 1.8 823750-901Narrow Bore 2.1 x 250 5 959790-918Narrow Bore 2.1 x 150 5 959701-902 959701-906 959701-912 959701-918Narrow Bore 2.1 x 50 5 959746-902 959746-906Narrow Bore RR 2.1 x 150 3.5 959763-902 959763-906 959763-912Narrow Bore RR 2.1 x 100 3.5 959793-902 959793-906 959793-912 959793-918Narrow Bore RR 2.1 x 50 3.5 959743-902 959743-906 959743-912Narrow Bore RR 2.1 x 30 3.5 959733-902 959733-906 959733-912Narrow Bore RRHD, 1200 bar 2.1 x 150 1.8 959759-902 959759-906Narrow Bore RRHD, 1200 bar 2.1 x 100 1.8 959758-902 959758-906Narrow Bore RRHD, 1200 bar 2.1 x 50 1.8 959757-902 959757-906Narrow Bore RRHT, 600 bar 2.1 x 100 1.8 959764-902 959764-906 959764-912 959764-918Narrow Bore RRHT, 600 bar 2.1 x 50 1.8 959741-902 959741-906 959741-912 959741-918Narrow Bore RRHT, 600 bar 2.1 x 30 1.8 959731-902 959731-906 959731-912UHPLC Guard, 1200 bar, 3/pk 2.1 x 5 1.8 821725-901Guard Cartridges, 4/pk 4.6 x 12.5 5 820950-936 820950-937 820950-938 820950-939Guard Cartridges, 4/pk 2.1 x 12.5 5 821125-936 821125-937 821125-938 821125-939Guard Hardware Kit 820999-901 820999-901 820999-901 820999-901


(µm)



Eclipse PlusPhenyl-HexylUSP L11

EclipsePAHUSP L1

ZORBAX Eclipse Plus

254


ZORBAX Eclipse PAH• High resolution separation of 16 PAHs in EPA Method 610• Extensive range of particle sizes (1.8, 3.5 and 5 µm) and sizes for fast and high resolution separations• Each batch of material is specifically tested with PAHs for maximum reproducibility under expected

operating conditions• Excellent performance using the high quality, improved silica of Eclipse Plus columns• Good for applications requiring "shape selectivity" or the separation of geometric isomers

Agilent ZORBAX Eclipse PAH columns are recommended for the separation of polycyclic aromatichydrocarbons. PAHs are considered priority pollutants and the analysis of these potentially carcinogeniccompounds in water, soil and food is of major importance. Eclipse PAH columns separate all 16 PAHS inEPA method 610 quickly and with high resolution.



SurfaceArea

temp.Limits pH Range Endcapped

CarbonLoad

ZORBAX Eclipse PAH 95Å 160 m2/g 60 °C 2.0-8.0 No 14%

Specifications represent typical values only.

LCEPlusPAHTime (min)

1 2 3 4 5

0

500

250

750

1250

1750

1000

1500

2000

mAU

High resolution and fast analysis on RRHt Eclipse PAH columnColumn: Eclipse PAH

959941-9184.6 x 50 mm, 1.8 µm

Mobile Phase: A: Water; B: Acetonitrile

Gradient: Time (Min) 0.00 3.5 5.2 5.5 6.5

% B401001004040


Temperature: 25 °C

Detector: DAD 220, 4 nm No Ref. DAD Stop Time = 6.0 minStop Time = 7.0

Rs = 2.2

Rs = 2.2 vs. 2.0 for4.6 x 50 mm, 3.5 µm

ZORBAX Eclipse PAH Columns



ZORBAX Eclipse PAH


(µm)

EclipsePAHUSP L1

Analytical 4.6 x 250 5 959990-918Analytical 4.6 x 150 5 959993-918Analytical 4.6 x 100 5 959996-918Rapid Resolution 4.6 x 150 3.5 959963-918Rapid Resolution 4.6 x 100 3.5 959961-918Rapid Resolution 4.6 x 50 3.5 959943-918Rapid Resolution HT, 600 bar 4.6 x 100 1.8 959964-918Rapid Resolution HT, 600 bar 4.6 x 50 1.8 959941-918Rapid Resolution HT, 600 bar 4.6 x 30 1.8 959931-918Solvent Saver 3.0 x 250 5 959990-318Narrow Bore 2.1 x 250 5 959790-918Narrow Bore 2.1 x 150 5 959701-918Narrow Bore RR 2.1 x 100 3.5 959793-918Narrow Bore RRHT, 600 bar 2.1 x 100 1.8 959764-918Narrow Bore RRHT, 600 bar 2.1 x 50 1.8 959741-918Guard Cartridges, 4/pk 4.6 x 12.5 5 820950-939Guard Cartridges, 4/pk 2.1 x 12.5 5 821125-939Guard Hardware Kit 820999-901

256


CH3

CH3

Si

CH3

CH3

CH3Si

CH3

CH3

CH3Si

CH3

CH3

Si

CH3

CH3

Si

O

O

O

O

O

ZORBAX Eclipse XDB• Four selectivity choices for method development optimization• Good peak shape for basic, acidic and neutral compounds• High performance over a wide pH range – pH 2-9• Particle sizes from 1.8 to 7 µm• Long lifetime with eXtra Dense Bonding and double endcapping

Agilent ZORBAX Eclipse XDB columns – C18, C8, Phenyl and CN – provide four bonded phase choices formethod development optimization. These columns provide good peak shape over a wide pH range (2-9) for additional method development flexibility with one family of columns. Eclipse XDB columns can be usedfor method development at low pH (2-3) and the same column can be used for method development in themid pH (6-8) region. In the mid pH region residual silanols are more active and tailing interactions are morelikely. To overcome these interactions, Eclipse XDB columns are eXtra Densely Bonded and doubleendcapped through a proprietary process to cover as many active silanols as possible. The result is superiorpeak shape of basic compounds from pH 2-9. Eclipse XDB columns are available in 1.8, 3.5, 5 and 7 µmparticle sizes for high speed, high resolution, analytical and prep scale separations.


Bonded PhasePoreSize Surface Area

temp.Limits

pHRange* Endcapped

CarbonLoad

ZORBAX Eclipse XDB-C18 80Å 180 m2/g 60 °C 2.0-9.0 Double 10%ZORBAX Eclipse XDB-C8 80Å 180 m2/g 60 °C 2.0-9.0 Double 7.6%ZORBAX Eclipse XDB-Phenyl 80Å 180 m2/g 60 °C 2.0-9.0 Double 7.2%ZORBAX Eclipse XDB-CN 80Å 180 m2/g 60 °C 2.0-8.0 Double 4.3%

Specifications represent typical values only*Eclipse XDB columns are designed for operation over a wide pH range.At pH 6-9, highest columns stability for all silicabased columns is achieved by operating at temperatures <40 °C and using low buffer concentrations in the range of 0.01-0.02 M.

eXtra Densely Bonded and Double EndcappedEclipse XDB Bonded Phase

Poroshell 120 EC-CN is very similar to ZORBAX XDB-CN. Page 228

tiPS & tOOLS



LCEC004

1

4

3

2

1

3

2

5

Time (min)

A B

0 2.5 5.0 7.5Time (min)

0 2.5 5.0 7.5

Eclipse XDB columns are stable over a wide pH range. At low pH an Eclipse endcapped column is extremely stable and shows equivalent stability to a non-endcapped column,SB-C8, at pH 3. The columns were purged with a pH 3 mobile phase at 60 °C. Then they were tested with a strongly basic compound to determine if the endcapping or bondedphase had been hydrolyzed from the silica surface. The Eclipse XDB column was very stable, as shown by the consistency of the retention of amitriptyline over the 12,000 columnvolumes of the test. Another endcapped column shows less stability under these same conditions.

Column stability testing at pH 3 and 60 °CColumn: ZORBAX SB-C8

883975-9064.6 x 150 mm, 5 µm

Column: Eclipse XDB-C8993967-9064.6 x 150 mm, 5 µm

Mobile Phase: Purge Conditions:70% 50 mM NaAc-HCl, pH 3.030% ACNRetention Test Conditions:65% Methanol35% Water


Temperature: 60 °C

Sample: Tricyclic antidepressants

good peak shape over a wide pH range with ZORBAX Eclipse XDBColumn: Eclipse XDB-C8

993967-9064.6 x 150 mm, 5 µm

Mobile Phase: A: pH 3.0 75% 25 mM phosphate buffer 25% ACNB: pH 7.0 90% 20 mM phosphate 10% ACN


Temperature: 40 °C

Sample: A: 1. Maleate2. Doxylamine3. Chlorpheniramine4. Triprolidine5. DiphenhydramineB: 1. Procainamide2. N-acetylprocainamide3. N-propionylprocainamideZORBAX Eclipse XDB columns provide good peak shape over a wide pH

range and are an excellent choice for method development from pH 2-9.

LCEC005Column Volumes of Mobile Phase (X1000)

K of

Am

itrip

tylin

e

0 25.0

5.5

6.0

6.5

7.0

4 6 8 1210

ZORBAX SB-C8

ZORBAX Eclipse XDB-C8

Competitive C8

258


LCEC006

1

4

5

2, 3

1

4

5

2

Time (min)

A B

10 11 120 1 2 3 4 5 6 7 8 9Time (min)

0 1 2 3 4 5 6 7 8

3

Double endcapping, dense bonding and the durable Rx-Sil particles (sol-type) combine to provide long lifetime at pH 7 when compared to single endcapped sil-gel columns used here. The conditions used for this test – high temperature (60 °C) and high salt concentration (250 mM), accelerate the dissolution of silica, causing premature failure of the sil-gel type column.

Column stability testing at pH 7.0Column A: Competitive C8

SiL-typeAfter 1826 column volumes

Column B: Eclipse XDB-C8993967-9064.6 x 150 mm, 5 µmSol-typeAfter 1843 column volumes

Mobile Phase: 60% ACN40% 250 mM Phosphate Buffer, pH 7.0


Temperature: 60 °C

Sample: Tricyclic antidepressants

1. Uracil2. Nortriptyline3. Doxepin4. Amitriptyline5. Trimipramine

LCEC008

1

3

2

1

3

2

Time (min)

A B

0 0.5 1.0 1.5 2.0 2.5 3.0 3.5 4.0 4.5Time (min)

0 0.5 1.0 1.5 2.0 2.5 3.0 3.5 4.0 4.5

Eclipse XDB and StableBond columns are based on the same silica but have different bonding and endcapping. Therefore, they can have very different selectivity for the samesample under the same conditions, as this example shows.

Selectivity changes for basic compounds with Eclipse XDB and StableBondColumn A: Eclipse XDB-C8

966967-9064.6 x 75 mm, 3.5 µm

Column B: ZORBAX Rx/SB-C8866953-9064.6 x 75 mm, 3.5 µm

Mobile Phase: 70% 25 mM NaH2PO4, pH 3.030% Methanol


Temperature: 35 °C

1. Barbital2. Sulfamethoxazole3. Caffeine



LCEC007

1

3

2

1

3

2

1

3

2

Time (min)10 12 14 160 2 4 6 8

10 12 14 160 2 4 6 8

10 12 14 160 2 4 6 8

A

B

C

This separation of sunscreens on all three Eclipse XDB bonded phases – C18, C8 and Phenyl – shows that different bonded phases can be used to optimize a separation. While allthree bonded phases provide an adequate separation, the Eclipse XDB-Phenyl provides a different peak elution order and a much shorter overall analysis time. All three bondedphases also provide excellent peak shape with no mobile phase additives.

Optimize separations with Eclipse XDBselectivity optionsColumn A: Eclipse XDB-Phenyl

963967-9124.6 x 150 mm, 3.5 µm

Column B: Eclipse XDB-C8963967-9064.6 x 150 mm, 3.5 µm

Column C: Eclipse XDB-C18963967-9024.6 x 150 mm, 3.5 µm

Mobile Phase: 15% H2O:85% MeOH


Temperature: 35 °C

Sample: Sunscreens

1. Oxybenzone2. Padimate-O3. Ethylhexylsalicylate

The Eclipse XDB-CN column reduces retention time and provides good selectivity for Urea pesticides when compared to an Eclipse XDB-C18 column.

Selectivity for urea pesticidesColumn A: Eclipse XDB-C18

993967-9024.6 x 150 mm, 5 µm

Column B: Eclipse XDB-Cn993967-9054.6 x 150 mm, 5 µm

Column C: Eclipse XDB-C18993967-9024.6 x 150 mm, 5 µm

Mobile Phase: A. 60:40 MeOH:WaterB. 60:40 MeOH:WaterC. 77:23 MeOH:Water


Temperature: 25 °C

Sample: Urea pesticidesLCEC010

13

2

6

6

4

5

1

3

24

5

61

32

45

Time (min)

Time (min)

A

B

0 10

0 2 4 6 8 10

Time (min)

C

0 2 4 6 8 10

20 30 40 50

1. Fenuron2. Monuron3. MonoLinuron4. Diuron5. Linuron6. Pencycuron

260


(Continued)

ZORBAX Eclipse XDB

Hardware Description Size (mm) Particle Size (µm)

EclipseXDB-C18USP L1

EclipseXDB-C8USP L7

EclipseXDB-PhenylUSP L11

EclipseXDB-CnUSP L10

Standard Columns (no special hardware required)Semi-Preparative 9.4 x 250 5 990967-202 990967-206Analytical 4.6 x 250 5 990967-902 990967-906 990967-912 990967-905Analytical 4.6 x 150 5 993967-902 993967-906 993967-912 993967-905Analytical 4.6 x 50 5 946975-902 946975-906Rapid Resolution 4.6 x 150 3.5 963967-902 963967-906 963967-912 963967-905Rapid Resolution 4.6 x 100 3.5 961967-902 961967-906 961967-905Rapid Resolution 4.6 x 75 3.5 966967-902 966967-906 966967-912 966967-905Rapid Resolution 4.6 x 50 3.5 935967-902 935967-906 935967-912Rapid Resolution 4.6 x 30 3.5 934967-902 934967-906Rapid Resolution 4.6 x 20 3.5 932967-902 932967-906UHPLC Guard, 1200 bar, 3/pk 4.6 x 5 1.8 820750-903Rapid Resolution HT, 600 bar 4.6 x 100 1.8 928975-902 928975-906Rapid Resolution HT, 600 bar 4.6 x 50 1.8 927975-902 927975-906Rapid Resolution HT, 600 bar 4.6 x 30 1.8 924975-902 924975-906Rapid Resolution HT, 600 bar 4.6 x 20 1.8 926975-902 926975-906Solvent Saver 3.0 x 250 5 990967-302 990967-306 990967-312 990967-305Solvent Saver 3.0 x 150 5 993967-302 993967-306 993967-312 993967-305Solvent Saver Plus 3.0 x 150 3.5 963954-302 963954-306 963954-312 963954-305Solvent Saver Plus 3.0 x 100 3.5 961967-302 961967-306 961967-312Solvent Saver Plus 3.0 x 75 3.5 966954-302Solvent Saver RRHD, 1200 bar 3.0 x 150 1.8 981759-302Solvent Saver RRHD, 1200 bar 3.0 x 100 1.8 981758-302Solvent Saver RRHD, 1200 bar 3.0 x 50 1.8 981757-302Solvent Saver HT, 600 bar 3.0 x 100 1.8 928975-302 928975-306Solvent Saver HT, 600 bar 3.0 x 50 1.8 927975-302 927975-306Solvent Saver HT, 600 bar 3.0 x 30 1.8 924975-302 924975-306Solvent Saver HT, 600 bar 3.0 x 20 1.8 926975-302 926975-306UHPLC Guard, 1200 bar, 3/pk 3.0 x 5 1.8 823750-903Narrow Bore 2.1 x 150 5 993700-902 993700-906 993700-912 993700-905Narrow Bore 2.1 x 50 5 960967-902 960967-906 960967-912 960967-905Narrow Bore RR 2.1 x 150 3.5 930990-902 930990-906

Unless indicated, column pressure limit is 400 bar.*These columns are packed with Eclipse XDB-C18, 5 µm.



Narrow Bore RR 2.1 x 100 3.5 961753-902 961753-906 961753-905Narrow Bore RR 2.1 x 75 3.5 966735-902Narrow Bore RR 2.1 x 50 3.5 971700-902 971700-906Narrow Bore RR 2.1 x 30 3.5 974700-902 974700-906Narrow Bore RR 2.1 x 20 3.5 972700-902 972700-906Narrow Bore RRHD, 1200 bar 2.1 x 150 1.8 981759-902Narrow Bore RRHD, 1200 bar 2.1 x 100 1.8 981758-902Narrow Bore RRHD, 1200 bar 2.1 x 50 1.8 981757-902Narrow Bore RRHT, 600 bar 2.1 x 100 1.8 928700-902 928700-906Narrow Bore RRHT, 600 bar 2.1 x 50 1.8 927700-902 927700-906Narrow Bore RRHT, 600 bar 2.1 x 30 1.8 924700-902 924700-906Narrow Bore RRHT, 600 bar 2.1 x 20 1.8 926700-902 926700-906UHPLC Guard, 1200 bar, 3/pk 2.1 x 5 1.8 821725-903MicroBore RR 1.0 x 150 3.5 963600-902 963600-906MicroBore RR 1.0 x 50 3.5 965600-902 965600-906

ZORBAX Eclipse XDB



EclipseXDB-C8USP L7

EclipseXDB-PhenylUSP L11

EclipseXDB-CnUSP L10

Standard Columns (no special hardware required)

MicroBore RR 1.0 x 30 3.5 961600-902 961600-906MicroBore Guard, 3/pk 1.0 x 17 5 5185-5921 5185-5921Guard Cartridge 9.4 x 15 5 820675-112* 820675-112* 820675-112* 820675-112*Guard Cartridges, 4/pk 4.6 x 12.5 5 820950-925 820950-926 820950-927 820950-935Guard Cartridges, 4/pk 2.1 x 12.5 5 821125-926 821125-926 821125-926 821125-935Guard Hardware Kit 840140-901 840140-901 840140-901 840140-901Guard Hardware Kit 820999-901 820999-901 820999-901 820999-901

PrepHt Cartridge Columns (require endfittings kit 820400-901)PrepHT Cartridge 21.2 x 250 7 977250-102 977250-106PrepHT Cartridge 21.2 x 150 7 977150-102 977150-106PrepHT Cartridge 21.2 x 150 5 970150-902 970150-906PrepHT Cartridge 21.2 x 100 5 970100-902 970100-906PrepHT Cartridge 21.2 x 50 5 970050-902 970050-906PrepHT Guard Cartridge 17.0 x 7.5 5 820212-925 820212-926Guard Cartridge Hardware 820444-901 820444-901PrepHT Endfittings, 2/pk 820400-901 820400-901

Unless indicated, column pressure limit is 400 bar.*These columns are packed with Eclipse XDB-C18, 5 µm.

262


(Continued)

ZORBAX Eclipse XDB



EclipseXDB-C8USP L7

Agilent Cartridge Columns (require hardware kit 5021-1845)Analytical 4.6 x 250 5 7995118-585 7995108-585Analytical 4.6 x 150 5 7995118-595 7995108-595Rapid Resolution 4.6 x 75 3.5 7995118-344 7995108-344Solvent Saver Plus 3.0 x 75 3.5 7995230-344Guard Cartridges, 10/pk 4.0 x 4 5 7995118-504 7995118-504Cartridge Holder 5021-1845 5021-1845

Standard Columns (no special hardware required)Rapid Resolution HT, 400 bar 4.6 x 50 1.8 922975-902 922975-906Rapid Resolution HT, 3/pk, 400 bar 4.6 x 50 1.8 922975-932Narrow Bore RRHT, 400 bar 2.1 x 50 1.8 922700-902Narrow Bore RRHT, 3/pk, 400 bar 2.1 x 50 1.8 922700-932

Rapid Resolution Ht Cartridges (require hardware kit 820555-901)Rapid Resolution Cartridge 4.6 x 30 3.5 933975-902 933975-906Rapid Resolution Cartridge, 3/pk 4.6 x 30 3.5 933975-932 933975-936Rapid Resolution Cartridge 4.6 x 15 3.5 931975-902 931975-906Rapid Resolution Cartridge, 3/pk 4.6 x 15 3.5 931975-932 931975-936Rapid Resolution Cartridge 2.1 x 30 3.5 973700-902 973700-906Rapid Resolution Cartridge, 3/pk 2.1 x 30 3.5 973700-932 973700-936Rapid Resolution Cartridge 2.1 x 15 3.5 975700-902 975700-906Rapid Resolution Cartridge, 3/pk 2.1 x 15 3.5 975700-932 975700-936Rapid Resolution HT Cartridge, 400 bar 4.6 x 50 1.8 925975-902Rapid Resolution HT Cartridge, 3/pk, 400 bar 4.6 x 50 1.8 925975-932Rapid Resolution HT Cartridge, 400 bar 4.6 x 30 1.8 923975-902Rapid Resolution HT Cartridge, 3/pk, 400 bar 4.6 x 30 1.8 923975-932



Rapid Resolution HT Cartridge, 400 bar 4.6 x 15 1.8 921975-902Rapid Resolution HT Cartridge, 3/pk, 400 bar 4.6 x 15 1.8 921975-932Rapid Resolution HT Cartridge, 400 bar 2.1 x 50 1.8 925700-902Rapid Resolution HT Cartridge, 3/pk, 400 bar 2.1 x 50 1.8 925700-932Rapid Resolution HT Cartridge, 400 bar 2.1 x 30 1.8 923700-902Rapid Resolution HT Cartridge, 3/pk, 400 bar 2.1 x 30 1.8 923700-932Rapid Resolution HT Cartridge, 400 bar 2.1 x 15 1.8 921700-902Rapid Resolution HT Cartridge, 3/pk, 400 bar 2.1 x 15 1.8 921700-932Hardware Kit for RR and RRHT Cartridges 820555-901

Capillary glass-lined ColumnsCapillary 0.5 x 250 5 5064-8286Capillary 0.5 x 150 5 5064-8287Capillary RR 0.5 x 150 3.5 5064-8288Capillary RR 0.5 x 35 3.5 5064-8298Capillary 0.3 x 250 5 5064-8269Capillary 0.3 x 150 5 5064-8291Capillary RR 0.3 x 150 3.5 5064-8271Capillary 0.5 x 35 5 5064-8296Capillary 0.3 x 35 5 5064-8297

Rapid Resolution Ht Cartridges (require hardware kit 820555-901)Hardware Description Size (mm) Particle Size (µm)


EclipseXDB-C8USP L7

ZORBAX Eclipse XDB

264


R

R

R

R

R

R

R1SiO

OH

OH

R1SiO

R1SiO

ZORBAX 80Å StableBond• Longest column lifetime and best reproducibility for low pH separations – down to pH 1 • Patented stable column chemistry allows use at high temperature and low pH without degradation• Six different bonded phases provide broad selectivity – SB-C18, SB-C8, SB-CN, SB-Phenyl, SB-C3,

and SB-Aq• High purity (Type B) silica for good peak shape

Agilent ZORBAX StableBond columns use patented, unique, nonfunctional silanes with bulky diisobutyl (SB-C18) or diisopropyl (SB-C8, SB-C3, SB-Phenyl, SB-CN, and SB-Aq) side chain groups that stericallyprotect the key siloxane bond to the silica surface from hydrolytic attack at low pH. StableBond packingmaterials are not endcapped in order to provide exceptional stability and to maximize lifetime andreproducibility under acidic mobile phase conditions. The high purity, low acidity silica provides excellentpeak shape with acidic, basic and neutral compounds making StableBond columns an excellent choice forlow pH method development. ZORBAX StableBond columns are compatible with all common mobilephases, including very high aqueous mobile phases.



SurfaceArea

temp.Limits* pH Range* Endcapped

CarbonLoad

ZORBAX SB-C18 80Å 180 m2/g 90 °C 0.8-8.0 No 10%ZORBAX SB-C8 80Å 180 m2/g 80 °C 1.0-8.0 No 5.5%ZORBAX SB-C3 80Å 180 m2/g 80 °C 1.0-8.0 No 4%ZORBAX SB-Phenyl 80Å 180 m2/g 80 °C 1.0-8.0 No 5.5%ZORBAX SB-CN 80Å 180 m2/g 80 °C 1.0-8.0 No 4%ZORBAX SB-Aq 80Å 180 m2/g 80 °C 1.0-8.0 No proprietary

Specifications represent typical values only*StableBond columns are designed for optimal use at low pH. At pH 6-8, highest column stability for all silica-based columnsis obtained by operating at temperatures <40 °C and using lower buffer concentrations in the range of 0.01-0.02 M. Atmid-range pH, Eclipse Plus, Eclipse XDB and Bonus-RP are recommended.

tiPS & tOOLS

ZORBAX StableBond SB-C18, SB-C8 and SB-Aq phases are also available on Poroshell 120.Turn to page 228

Sterically Protected StableBond Bonded Phase



As an indicator of column breakdown, retention timeof toluene was measured after purging the columnwith mobile phase. Only the StableBond SB-C18 isunchanged after three working months of use underthese very low pH (0.8) and high temperature (90 °C)conditions. ZORBAX Rx-C18 also provides a stablematrix, and can be used as an alternative selectivity to StableBond SB-C18.

StableBond SB-C18 shows excellent stability at low pH and high temperature (pH 0.8, 90 °C)Column: ZORBAX SB-C18

883975-9024.6 x 150 mm, 5 µm

Column: ZORBAX Rx-C18883967-9024.6 x 150 mm, 5 µm

Mobile Phase: 50% Methanol/50% Waterwith 1.0% TFATest Solute: Toluene

Temperature: 90 °C

ZORBAX StableBond SB-CN and other short chain StableBond bondedphases are also exceptionally stable at low pH. Conventional dimethylCN and similar bonded phases lack this stability.

Shorter chain ZORBAX SB-Cn is also stable at low pH (pH 2.0, 50 °C)Column: ZORBAX SB-Cn

883975-9054.6 x 150 mm, 5 µm

Mobile Phase: 0.1% TFA, pH 2:ACN

Flow Rate: 1 mL/min

Gradient: 0-100% ACN

Temperature: 50 °C

Sample: 1-phenylheptane @ 50% AC/50% water with 0.1% TFA

LCSB002Column Volumes

% k

Rem

aini

ng

0 1,000 2,000 3,000 4,000 5,000 6,0000

20

40

60

80

100SB-CN

Si-(Me)2PrCN

StableBond SB-C18(Diisobutyl-C18)

ZORBAX Rx-C18 (Dimethyl-C18)

Competitor A-C18

Competitor B-C18

Competitor C-C18

Competitor D-C18

Competitor E-C18

LCSB001Column Volumes of Mobile Phase Purge

Relat

ive R

eten

tion

0 5,000 10,000 15,000 20,000 25,000 30,0000.0

0.2

0.4

0.6

0.8

1.0

266


LCSB003

1

3

2

4

5

13

2

4

5

Time (min)

A B

0 5 20 251510Time (min)

0 2 4 6 8 1210

The SB-CN column is used here to reduce analysis time by 50%. The retention of the most hydrophobic analyte is cut in half. At the same time, retention of the more polar, earlyeluting peaks increases slightly.

SB-Cn optimizes retention and resolutionColumn A: ZORBAX SB-C18

866953-9024.6 x 75 mm, 3.5 µm

Column B: ZORBAX SB-Cn866953-9054.6 x 75 mm, 3.5 µm

Mobile Phase: 30% ACN70% 25mM NaH2PO4, pH 2.5


Temperature: 35 °C

1. Estriol2. Daidzen3. Quercetin4. Genistein5. Diethylstilbestrol

SB-C3 is just one of the five different StableBond selectivity choices. In this example,optimum resolution is obtained with SB-C3. All are based on the same high purity Rx-SIL.Selectivity changes are therefore dependent only on the bonded phases, making methoddevelopment more reliable.

five different bonded phases provide selectivity optionsColumn A: ZORBAX SB-C18

883975-9024.6 x 150 mm, 5 µm

Column B: ZORBAX SB-C8883975-9064.6 x 150 mm, 5 µm

Column C: ZORBAX SB-C3883975-9094.6 x 150 mm, 5 µm

Column D: ZORBAX SB-Phenyl883975-9124.6 x 150 mm, 5 µm

Column E: ZORBAX SB-Cn883975-9054.6 x 150 mm, 5 µm

Mobile Phase: 0-100% B in 18.8 minA: 50 mM NaH2PO4,pH 2.5 in 95% H2O / 5% ACNB: 50 mM NaH2PO4,pH 2.5 in 47% H2O / 53% ACN


Temperature: 26 °C

Detector: 254 nm

LCSB004

13

2

4

5

1

3

2

4

5

1

3

2

4

5

1

3

2

4

5

1 3

2 45

Time (min)

A

B

C

D

E

0 5 1510

Sample: 1. Procaine2. Lidocaine3. d-Cinchonine4. Butacaine5. Tetracaine



(Continued)

ZORBAX 80Å StableBond

Hardware Description Size (mm)Particle

Size (µm)SB-C18USP L1

SB-C8USP L7

SB-CnUSP L10

SB-C3USP L56

SB-PhenylUSP L11 SB-Aq

Standard Columns (no special hardware required)Semi-Preparative 9.4 x 250 5 880975-202 880967-201 880975-205 880975-209 880975-212Semi-Preparative 9.4 x 150 5 883975-202Semi-Preparative 9.4 x 100 5 884975-202Semi-Preparative 9.4 x 50 5 846975-202Analytical 4.6 x 250 5 880975-902 880975-906 880975-905 880975-909 880975-912 880975-914Analytical 4.6 x 150 5 883975-902 883975-906 883975-905 883975-909 883975-912 883975-914Analytical 4.6 x 50 5 846975-902 846975-906 846975-914Rapid Resolution 4.6 x 250 3.5 884950-567Rapid Resolution 4.6 x 150 3.5 863953-902 863953-906 863953-905 863953-912 863953-914Rapid Resolution 4.6 x 100 3.5 861953-902 861953-906 861953-905 861953-912 861953-914Rapid Resolution 4.6 x 75 3.5 866953-902 866953-906 866953-905 866953-912 866953-914Rapid Resolution 4.6 x 50 3.5 835975-902 835975-906 835975-905 835975-912 835975-914Rapid Resolution 4.6 x 30 3.5 834975-902 834975-906Rapid Resolution 4.6 x 20 3.5 832975-902 832975-906Rapid Resolution HT, 600 bar 4.6 x 150 1.8 829975-902 829975-906 829975-905 829975-912 829975-914Rapid Resolution HT, 600 bar 4.6 x 100 1.8 828975-902 828975-906 828975-905 828975-912 828975-914Rapid Resolution HT, 600 bar 4.6 x 75 1.8 830975-906Rapid Resolution HT, 600 bar 4.6 x 50 1.8 827975-902 827975-906 827975-905 827975-912 827975-914Rapid Resolution HT, 600 bar 4.6 x 30 1.8 824975-902 824975-906 824975-905 824975-912 824975-914Rapid Resolution HT, 600 bar 4.6 x 20 1.8 826975-902 826975-906UHPLC Guard, 600 bar, 3/pk 4.6 x 5 1.8 820750-902 820750-904Solvent Saver 3.0 x 250 5 880975-302 880975-306 880975-305 880975-309 880975-312 880975-314Solvent Saver 3.0 x 150 5 883975-302 883975-306 883975-305 883975-309 883975-312 883975-314Solvent Saver Plus 3.0 x 150 3.5 863954-302 863954-306 863954-305 863954-312 863954-314Solvent Saver Plus 3.0 x 100 3.5 861954-302 861954-306 861954-305 861954-309 861954-312 861954-314Solvent Saver Plus 3.0 x 75 3.5 866953-302

Unless indicated, column pressure limit is 400 bar.

Solvent Saver RRHD, 1200 bar 3.0 x 150 1.8 859700-302 859700-306

Solvent Saver RRHD, 1200 bar 3.0 x 100 1.8 858700-302 858700-306 858700-305 858700-312

Solvent Saver RRHD, 1200 bar 3.0 x 50 1.8 857700-302 857700-306 857700-305 857700-312

Solvent Saver HT, 600 bar 3.0 x 150 1.8 829975-302 829975-306 829975-305 829975-312Solvent Saver HT, 600 bar 3.0 x 100 1.8 828975-302 828975-306 828975-305 828975-309 828975-312 828975-314Solvent Saver HT, 600 bar 3.0 x 50 1.8 827975-302 827975-306 827975-305Solvent Saver HT, 600 bar 3.0 x 30 1.8 824975-302 824975-306 824975-305 827975-312 827975-314Solvent Saver HT, 600 bar 3.0 x 20 1.8 826975-302 826975-306UHPLC Guard, 1200 bar, 3/pk 3.0 x 5 1.8 823750-902 823750-904Narrow Bore 2.1 x 150 5 883700-922 883700-906 883700-905 883700-909 883700-912Narrow Bore 2.1 x 50 5 860975-902 860975-906 860975-905 860975-909 860975-912 860975-914Narrow Bore RR 2.1 x 150 3.5 830990-902 830990-906 830990-914Narrow Bore RR 2.1 x 100 3.5 861753-902 861753-906 861753-905 861753-912 861753-914Narrow Bore RR 2.1 x 75 3.5 866735-902Narrow Bore RR 2.1 x 50 3.5 871700-902 871700-906 871700-914Narrow Bore RR 2.1 x 30 3.5 874700-902 874700-906Narrow Bore RR 2.1 x 20 3.5 872700-902 872700-906Narrow Bore RRHD, 1200 bar 2.1 x 150 1.8 859700-902 859700-906 859700-905 859700-912Narrow Bore RRHD, 1200 bar 2.1 x 100 1.8 858700-902 858700-906 858700-905 858700-912

268


(Continued)



Size (µm)SB-C18USP L1

SB-C8USP L7

SB-CnUSP L10

SB-C3USP L56



Narrow Bore RRHD, 1200 bar 2.1 x 50 1.8 857700-902 857700-906 857700-905 857700-912Unless indicated, column pressure limit is 400 bar.



Narrow Bore RRHT, 600 bar 2.1 x 150 1.8 820700-902 820700-906 820700-905 820700-912Narrow Bore RRHT, 600 bar 2.1 x 100 1.8 828700-902 828700-906 828700-905 828700-912 828700-914Narrow Bore RRHT, 600 bar 2.1 x 50 1.8 827700-902 827700-906 827700-905 827700-912 827700-914Narrow Bore RRHT, 600 bar 2.1 x 30 1.8 824700-902 824700-906 824700-905 824700-912 824700-914Narrow Bore RRHT, 600 bar 2.1 x 20 1.8 826700-902 826700-906UHPLC Guard, 1200 bar, 3/pk 2.1 x 5 1.8 821725-902 821725-904MicroBore RR 1.0 x 150 3.5 863600-902 863600-906 863600-905MicroBore RR 1.0 x 50 3.5 865600-902 865600-906MicroBore RR 1.0 x 30 3.5 861600-902 861600-906MicroBore Guard, 3/pk 1.0 x 17 5 5185-5920 5185-5920Guard Cartridge, 2/pk 9.4 x 15 7 820675-115 820675-115 820675-124 820675-124 820675-115Guard Cartridge, 4/pk 4.6 x 12.5 5 820950-920 820950-915 820950-916 820950-922 820950-917 820950-933Guard Cartridge, 4/pk 2.1 x 12.5 5 821125-915 821125-915 821125-924 821125-924 821125-915 821125-933Guard Hardware Kit 9.4 x 15 0 840140-901 840140-901 840140-901 840140-901 840140-901Guard Hardware Kit 820999-901 820999-901 820999-901 820999-901 820999-901 820999-901

PrepHt Cartridge Columns (require endfittings kit 820400-901)PrepHT Cartridge 21.2 x 250 7 877250-102 877250-106 877250-105 877250-112 877250-114PrepHT Cartridge 21.2 x 150 7 877150-102 877150-106 877150-114PrepHT Cartridge 21.2 x 150 5 870150-902 870150-906 870150-914PrepHT Cartridge 21.2 x 100 5 870100-902 870100-906 870100-914PrepHT Cartridge 21.2 x 50 5 870050-902 870050-906 870050-914PrepHT Guard Cartridge, 2/pk 17.0 x 7.5 5 820212-920 820212-915 820212-915 820212-915 820212-933Guard Cartridge Hardware 820444-901 820444-901 820444-901 820444-901 820444-901 820444-901PrepHT Endfittings, 2/pk 820400-901 820400-901 820400-901 820400-901 820400-901 820400-901


Standard Columns (no special hardware required)Hardware Description Size (mm)

ParticleSize (µm)

SB-C18USP L1

SB-C8USP L7

SB-CnUSP L10

SB-C3USP L56



270


Agilent Cartridge Columns (require hardware kit 5021-1845)Analytical 4.6 x 250 5 7995218-585 7995208-585Analytical 4.6 x 150 5 7995218-595 7995208-595Rapid Resolution 4.6 x 75 3.5 7995218-344 7995208-344Guard Cartridges, 10/pk 4.0 x 4 5 7995118-504 7995118-504Cartridge Holder 5021-1845 5021-1845

Standard Columns (no special hardware required)Rapid Resolution HT 4.6 x 50 1.8 822975-902 822975-906Rapid Resolution HT, 3/pk 4.6 x 50 1.8 822975-932Narrow Bore RRHT 2.1 x 50 1.8 822700-902Narrow Bore RRHT, 3/pk 2.1 x 50 1.8 822700-932

Rapid Resolution Cartridges (require hardware kit 820555-901)Rapid Resolution Cartridge 4.6 x 30 3.5 833975-902 833975-906 833975-912Rapid Resolution Cartridge, 3/pk 4.6 x 30 3.5 833975-932 833975-936Rapid Resolution Cartridge 4.6 x 15 3.5 831975-902 831975-906Rapid Resolution Cartridge, 3/pk 4.6 x 15 3.5 831975-932 831975-936Rapid Resolution Cartridge 2.1 x 30 3.5 873700-902 873700-906Rapid Resolution Cartridge, 3/pk 2.1 x 30 3.5 873700-932 873700-936Rapid Resolution Cartridge 2.1 x 15 3.5 875700-902 875700-906Rapid Resolution Cartridge, 3/pk 2.1 x 15 3.5 875700-932 875700-936

Rapid Resolution Ht Cartridges (require hardware kit 820555-901)Rapid Resolution HT Cartridge 4.6 x 50 1.8 825975-902Rapid Resolution HT Cartridge, 3/pk 4.6 x 50 1.8 825975-932Rapid Resolution HT Cartridge 4.6 x 30 1.8 823975-902Rapid Resolution HT Cartridge, 3/pk 4.6 x 30 1.8 823975-932Rapid Resolution HT Cartridge 4.6 x 15 1.8 821975-902Rapid Resolution HT Cartridge, 3/pk 4.6 x 15 1.8 821975-932Rapid Resolution HT Cartridge 2.1 x 50 1.8 825700-902Rapid Resolution HT Cartridge, 3/pk 2.1 x 50 1.8 825700-932Rapid Resolution HT Cartridge 2.1 x 30 1.8 823700-902Rapid Resolution HT Cartridge, 3/pk 2.1 x 30 1.8 823700-932Rapid Resolution HT Cartridge 2.1 x 15 1.8 821700-902Rapid Resolution HT Cartridge, 3/pk 2.1 x 15 1.8 821700-932Hardware Kit for RR and RRHT Cartridges 820555-901

Hardware Description Size (mm) Particle Size (µm)SB-C18USP L1

SB-C8USP L7

SB-PhenylUSP L11





Description Size (mm) Particle Size (µm)SB-C18USP L1

Capillary glass-lined ColumnsCapillary 0.5 x 250 5 5064-8258Capillary 0.5 x 150 5 5064-8256Capillary 0.5 x 35 5 5064-8254Capillary RR 0.5 x 150 3.5 5064-8262Capillary RR 0.5 x 35 3.5 5064-8260Capillary 0.3 x 250 5 5064-8257Capillary 0.3 x 150 5 5064-8255Capillary 0.3 x 35 5 5064-8253Capillary RR 0.3 x 150 3.5 5064-8261

272


ZORBAX Rx



SurfaceArea

temp. Limits

pHRange* Endcapped

CarbonLoad

ZORBAX Rx-C18 80Å 180 m2/g 60 °C 2.0-8.0 No 12%ZORBAX Rx-C8 80Å 180 m2/g 80 °C 1.0-8.0 No 5.5%

Specifications represent typical values only*At pH 6-9 highest column stability for all silica based columns is obtained by operating at temperatures <40 °C and usinglower buffer concentrations in the range of 0.01-0.02 M.

Analysis of diazepam on Rx-C18Column: ZORBAX Rx-C18

880967-3023.0 x 250 mm, 5 µm

Mobile Phase: 35% H2O:65% MeOH


LCRX001

Time (min)5.02.50.0 7.5

1

2

1. Ethylparaben2. Diazepam

• Recommended for alternate selectivity at low pH relative to Eclipse Plus C18, Eclipse XDB-C18 andStableBond SB-C18; for higher temperature applications, StableBond is recommended

• Higher carbon load than SB-C18 columns (12% vs. 10%)• High stability and good peak shape for low pH applications (up to pH 8)• Manufactured using dimethyloctadecylsilane and non-endcapped• ZORBAX Rx-C8 is the same product as SB-C8

An Rx-C18 column is used for this USP analysis of diazepam and the internal standardethylparaben. The Solvent Saver 3.0 mm id Rx-C18 column reduces solvent usage by 60%over what would be used if the analysis was done on a 4.6 x 250 mm column.



ZORBAX Rx


(µm)Rx-C18USP L1

Rx-C8USP L7*

Semi-Preparative 9.4 x 250 5 880967-202 880967-201Analytical 4.6 x 250 5 880967-902 880967-901Analytical 4.6 x 150 5 883967-902 883967-901Rapid Resolution 4.6 x 150 3.5 863967-902Rapid Resolution 4.6 x 100 3.5 861967-902Rapid Resolution 4.6 x 75 3.5 866967-902Solvent Saver 3.0 x 250 5 880967-302Solvent Saver 3.0 x 150 5 883967-302Solvent Saver Plus 3.0 x 150 3.5 863967-302Solvent Saver Plus 3.0 x 100 3.5 861967-302Narrow Bore 2.1 x 150 5 883700-902Narrow Bore RR 2.1 x 100 3.5 861767-902Guard Cartridge, 2/pk 9.4 x 15 7 820675-115 820675-115Guard Cartridge, 4/pk 4.6 x 12.5 5 820950-914 820950-913Guard Cartridge, 4/pk 2.1 x 12.5 5 821125-915 821125-915Guard Hardware Kit 9.4 x 15 840140-901 840140-901Guard Hardware Kit 820999-901 820999-901

PrepHt Cartridge Columns (require endfittings kit 820400-901)PrepHT Cartridge 21.2 x 250 7 877967-102 877250-106PrepHT Cartridge 21.2 x 150 7 877150-106PrepHT Cartridge 21.2 x 150 5 870150-906PrepHT Cartridge 21.2 x 100 5 870100-906PrepHT Cartridge 21.2 x 50 5 870050-906PrepHT Guard Cartridge, 2/pk 5 820212-914 820212-915Guard Cartridge Hardware 820444-901 820444-901PrepHT Endfittings, 2/pk 820400-901 820400-901

*Rx-C8 is the same product as SB-C8. For other sizes and configurations, see the ZORBAX StableBond section, page 264.

274


ZORBAX 80Å Extend-C18• High efficiency and long life at high pH – up to pH 11.5• Unique bidentate bonding and double endcapping provides high pH stability• More efficiency and better peak shape than polymer-based columns• Improve retention, resolution and peak shape of basic compounds• High sensitivity for LC/MS separations of peptides

The Agilent ZORBAX Extend-C18 column uses a novel bidentate C18-C18 bonding technology tomake it possible to develop high-resolution separations at high pH with a silica-based column. At high pH, non-charged basic compounds will not interact with the underlying silica. The result is high efficiency separations with superior peak shape and improved resolution. High pH separationsare also the best choice for compounds that are more stable or more soluble in high pH solutions.Some of the mobile phase buffer options for high pH include triethylamine, pyrrolidine, glycine, borateand ammonium hydroxide. Ammonium hydroxide at pH 10.5 is an excellent mobile phase modifier forthe LC/MS of peptides and small molecules with improved sensitivity compared with TFA containingmobile phase at low pH. The Extend-C18 column is stable from pH 2-11.5 with good peak shape forall types of compounds. Extend-C18 columns also provide an additional selectivity choice at low pH.



SurfaceArea

temp.Limits* pH Range** Endcapped

CarbonLoad

ZORBAX Extend-C18 80Å 180 m2/g 60 °C 2.0-11.5 Double 12.5%

Specifications represent typical values only.*Temperature limits are 60 °C up to pH 8, 40 °C from pH 8-11.5.**Above pH 6 highest column stability for all silica based columns is obtained by reducing the operating temperature to

40 °C or below and using lower buffer concentrations (0.01-0.02 M) or organic buffers.

OSi

C18

C18

Silica Support

SiO

tiPS & tOOLS

Always use Agilent Certified Lampsfor Best LC Performance

Agilent detector lamps are built to thetightest specifications and qualitystandards. They are designed to increaselight intensity and decrease noise, whichimproves chromatographic results. Agilent rigorously tests its lamps for lowest lamp-to-lamp variability. Trust Agilent lamps for robust, long-lasting performance and lower cost of ownership. To learn more, visitwww.agilent.com/chem/lamps



LC80001

1

3

4

5

6

7

2

1

4

5

6

7

2, 3

Time (min)0 5

Time (min)0 5

10

LC80002Volume Eluent (L)

Amou

nt o

f Diss

olve

d Si

lica

(mg)

0 15123 5 90

10

20

30

Pseudoephedrine and scopolamine are difficult to retain at low and mid pH. Pseudoephedrine isoften analyzed by ion exchange methods. The Extend-C18 column retains these compounds in anoncharged form at high pH and improves resolution.

Basic antihistamines on Extend-C18 at high pHColumn: ZORBAX Extend-C18

773450-9024.6 x 150 mm, 5 µm

Mobile Phase: pH 7:30% 20 mM Na2HPO4 70% MeOHpH 11:30% 20 mM TEA 70% MeOH



Detector: 254 nm

Sample: Antihistamines

1. Maleate2. Scopolamine3. Pseudoephedrine4. Doxylamine5. Chlorpheniramine6. Triprolidine7. Diphenhydramine

At high pH, columns will fail due to silica dissolution. The example here showsextended lifetime of ZORBAX Extend-C18 at high pH in comparison to competitorW. This was measured by the amount of dissolved silica.

Long life at high pH with Extend-C18Column: ZORBAX Extend-C18

773450-9024.6 x 150 mm, 5 µm

Mobile Phase: 20% Methanol80% 0.1 M Carbonate buffer, pH 10.0



pH 11

pH 7

ZORBAX Extend-C18

Competitor w

276


These basic compounds are separated on the Extend-C18 at low pH withexcellent peak shape. The Extend-C18 column can be used at high and low pH.

Extend-C18 provides good peak shape at low pHColumn: ZORBAX Extend-C18

773450-9024.6 x 150 mm, 5 µm

Mobile Phase: 80% 25 mM NaH2PO4, pH 3.020% Methanol


Temperature: 35 °C


Sample: Basic compounds

LC80003

1

2

3

4

Time (min)2 310 4 5 76

1. Theobromine2. Dimethylxanthine3. Theophylline4. Caffeine

(Continued)

ZORBAX 80Å Extend-C18


(µm)Extend-C18USP L1

Standard Columns (no special hardware required)Analytical 4.6 x 250 5 770450-902Analytical 4.6 x 150 5 773450-902Analytical 4.6 x 50 5 746450-902Rapid Resolution 4.6 x 150 3.5 763953-902Rapid Resolution 4.6 x 100 3.5 764953-902Rapid Resolution 4.6 x 75 3.5 766953-902Rapid Resolution 4.6 x 50 3.5 735953-902Rapid Resolution HT, 600 bar 4.6 x 100 1.8 728975-902Rapid Resolution HT, 600 bar 4.6 x 50 1.8 727975-902Rapid Resolution HT, 600 bar 4.6 x 30 1.8 724975-902Rapid Resolution HT, 600 bar 4.6 x 20 1.8 726975-902Solvent Saver 3.0 x 250 5 770450-302Solvent Saver 3.0 x 150 5 773450-302Solvent Saver Plus 3.0 x 150 3.5 763954-302Solvent Saver Plus 3.0 x 100 3.5 764953-302Solvent Saver Plus 3.0 x 50 3.5 735954-302




Solvent Saver RRHD, 1200 bar 3.0 x 100 1.8 758700-302Solvent Saver RRHD, 1200 bar 3.0 x 50 1.8 757700-302Solvent Saver HT, 600 bar 3.0 x 100 1.8 728975-302Solvent Saver HT, 600 bar 3.0 x 50 1.8 727975-302Solvent Saver HT, 600 bar 3.0 x 30 1.8 724975-302Solvent Saver HT, 600 bar 3.0 x 20 1.8 726975-302Narrow Bore 2.1 x 150 5 773700-902Narrow Bore 2.1 x 50 5 760450-902Narrow Bore RR 2.1 x 100 3.5 761753-902Narrow Bore RR 2.1 x 50 3.5 735700-902Narrow Bore RRHD, 1200 bar 2.1 x 150 1.8 759700-902Narrow Bore RRHD, 1200 bar 2.1 x 100 1.8 758700-902Narrow Bore RRHD, 1200 bar 2.1 x 50 1.8 757700-902Narrow Bore RRHT, 600 bar 2.1 x 100 1.8 728700-902Narrow Bore RRHT, 600 bar 2.1 x 50 1.8 727700-902Narrow Bore RRHT, 600 bar 2.1 x 30 1.8 724700-902Narrow Bore RRHT, 600 bar 2.1 x 20 1.8 726700-902MicroBore RR 1.0 x 150 3.5 763600-902MicroBore RR 1.0 x 50 3.5 765600-902MicroBore RR 1.0 x 30 3.5 761600-902MicroBore Guard, 3/pk 1.0 x 17 5 5185-5923Guard Cartridge, 4/pk 4.6 x 12.5 5 820950-930Guard Cartridge, 4/pk 2.1 x 12.5 5 821125-930Guard Hardware Kit 820999-901

PrepHT Cartridge 21.2 x 150 5 770150-902PrepHT 21.2 x 100 5 770100-902PrepHT 21.2 x 50 5 770050-902PrepHT Endfittings, 2/pk 820400-901PrepHT Guard Cartridge, 2/pk 17.0 x 7.5 5 820212-930Guard Cartridge Hardware 820444-901


ZORBAX 80Å Extend-C18


(µm)Extend-C18USP L1

PrepHt Cartridge Columns (require endfittings kit 820400-901)


278


R1

CH3

CH3

CH3

CH3

CH3

CH3

Si

SiO

O

O PG

PG

PG

R

R

R

Si

Si

Si

R1

R1

R1

R1

R1

ZORBAX Bonus-RP• Excellent peak shape for challenging basic compounds at low and mid pH• Unique reversed-phase selectivity• Novel bonding technology with embedded polar group and steric protection• Usable in 100% aqueous mobile phases

The Agilent ZORBAX Bonus-RP column has a polar amide group embedded in a long alkyl chain. This novel bonding reduces interactions between basic compounds and the silica support, improving peak shape for the most difficult basic compounds. Peak shape and column lifetime are further improved by triple endcapping. In addition, diisopropyl side groups provide steric protection against acid hydrolysis for good lifetime at low pH. The Bonus-RP column provides an alternate selectivity to C18 and C8 alkylbonded phases.



SurfaceArea

temp.Limits* pH Range Endcapped

CarbonLoad

ZORBAX Bonus-RP 80Å 180 m2/g 60 °C 2.0-9.0 Triple 9.5%

Specifications represent typical values only.*Temperature limits are 60 °C up to pH 8, 40 °C from pH 8-9.

Unique, Polar Alkyl Bonus-RP Bonded Phase

tiPS & tOOLS

ZORBAX Bonus-RP is also available on Poroshell 120.Turn page 228



LCBR001

1

3

2

Time (min)100 1 2 3 4 5 6 7 8 9

TF1. 1.82. 1.73. 2.1 1. Doxylamine

2. Chlorpheniramine3. Triprolidine

LCBR002

1

3

2

Time (min)0 1 2 3 4 5 6

TF1. 1.12. 1.13. 1.1

Bonus-RP eliminates peak tailing of these basic compounds in comparison to a typical alkyl C8 bonded phase. In the mid-pH region, residual silanols can interact more stronglywith basic compounds to cause peak tailing. The polar group in the Bonus-RP bonded phase eliminates peak tailing of these basic compounds by reducing interactions withresidual silanols.

improved peak shape of basic compounds using Bonus-RPColumn: Alkyl-C8

4.6 x 150 mm, 5 µmMobile Phase: 75% 25 mM NH4OAc, pH 5.5

25% ACN


Temperature: 40 °C

Detector: 254 nm

Column: ZORBAX Bonus-RP883668-9014.6 x 150 mm, 5 µm

Mobile Phase: 80% 25 mM NH4OAc, pH 5.520% ACN


Temperature: 40 °C

Detector: 254 nm

Triple endcapping of Bonus-RP enhances stability at pH 7. Each 10,000column volume is equivalent to approximately one working month.

ZORBAX Bonus-RP is stable at low and mid pHColumn: ZORBAX Bonus-RP

883668-9014.6 x 150 mm, 5 µm

Mobile Phase: 60% 25 mMPhosphate Buffer,pH 7.0:40% ACN


Temperature: 23 °C

LCBR003Column Volume of Purge

Tolu

ene

Plat

e H

eigh

t, cm

0 5,000 10,000 15,000 20,000 25,000 30,000 35,0000.0010

0.0012

0.0014

0.0016

0.0018

Competitive alkyl/amideBonus-RP

1. Doxylamine2. Chlorpheniramine3. Triprolidine

280


LCBR004Column Volume of Purge

Tolu

ene

Plat

e H

eigh

t, cm

0 10,000 20,000 30,000 40,0000.0020

0.0025

0.0030

0.0035

0.0040

0.0045

0.0050

0.0055

Sterically protecting side groups provide good low pH stability and longer column lifetime than similar polar alkyl bonded phases.

Dimethyl-C18/amide, Bonus-RPColumn: ZORBAX Bonus-RP

883668-9014.6 x 150 mm, 5 µm

Mobile Phase: Aging:50% MeOH50% 0.1% TFATest:80% MeOH20% H2O


Temperature: Aging: 60 °CTest:23 °C

Dimethyl-C18/amideBonus-RP

Peak elution order can change dramatically when using Bonus-RP.In this example, the elution order of the first three peaks changes.

ZORBAX Bonus-RP provides unique selectivityColumn A: ZORBAX Bonus-RP

883668-9014.6 x 150 mm, 5 µm

Column B: Eclipse XDB-C8993967-9064.6 x 150 mm, 5 µm

Mobile Phase: 75% 25 mM Na Citrate, pH 625% MeOH



Detector: 254 nm

Sample: 3 µLCephalosporins

LCBR005

Time (min)0 2

5

0

10

1

2

3

4

1

2

3

4

15

mAu

4 6 8 10

Time (min)0 2

5

0

10

15

mAu

4 6 8 10

A

B

1. Cephalexin2. Cephaclor3. Cephuroxime4. Cephoxitin



ZORBAX Bonus-RP


(µm)Bonus-RPUSP L60

Standard Columns (no special hardware required)Analytical 4.6 x 250 5 880668-901Analytical 4.6 x 150 5 883668-901Rapid Resolution 4.6 x 250 3.5 884950-577Rapid Resolution 4.6 x 150 3.5 863668-901Rapid Resolution 4.6 x 100 3.5 864668-901Rapid Resolution 4.6 x 75 3.5 866668-901Rapid Resolution 4.6 x 50 3.5 835668-901Rapid Resolution HT, 600 bar 4.6 x 100 1.8 828668-901Rapid Resolution HT, 600 bar 4.6 x 75 1.8 830668-901Rapid Resolution HT, 600 bar 4.6 x 50 1.8 827668-901Solvent Saver 3.0 x 250 5 880668-301Solvent Saver 3.0 x 150 5 883668-301Solvent Saver Plus 3.0 x 150 3.5 863668-301Solvent Saver Plus 3.0 x 100 3.5 864668-301Solvent Saver HT, 600 bar 3.0 x 100 1.8 828668-301Solvent Saver HT, 600 bar 3.0 x 50 1.8 827668-301Rapid Resolution HD, 1200 bar 2.1 x 150 1.8 859768-901Rapid Resolution HD, 1200 bar 2.1 x 100 1.8 858768-901Rapid Resolution HD, 1200 bar 2.1 x 50 1.8 857768-901Narrow Bore 2.1 x 150 5 883725-901Narrow Bore 2.1 x 50 5 861971-901


(Continued)

ZORBAX Bonus-RP bonding is also available on Poroshell 120columns. Turn to page 228.

282


tiPS & tOOLS

Watch LC troubleshooting videos featuring Agilent chromatographic experts atwww.agilent.com/chem/lctroubleshooting

Narrow Bore RR 2.1 x 150 3.5 863700-901Narrow Bore RR 2.1 x 100 3.5 861768-901Narrow Bore RR 2.1 x 50 3.5 861700-901Narrow Bore RRHT, 600 bar 2.1 x 100 1.8 828768-901Narrow Bore RRHT, 600 bar 2.1 x 50 1.8 827768-901MicroBore RR 1.0 x 150 3.5 863608-901MicroBore RR 1.0 x 50 3.5 865608-901MicroBore RR 1.0 x 30 3.5 861608-901MicroBore Guard, 3/pk 1.0 x 17 5 5185-5922Guard Cartridge, 4/pk 4.6 x 12.5 5 820950-928Guard Cartridge, 4/pk 2.1 x 12.5 5 821125-928Guard Hardware Kit 820999-901

PrepHt Cartridge Columns (require endfittings kit 820400-901)PrepHT Cartridge 21.2 x 250 7 878250-101PrepHT Cartridge 21.2 x 150 7 878150-101PrepHT Cartridge 21.2 x 150 5 868150-901PrepHT Cartridge 21.2 x 100 5 868100-901PrepHT Cartridge 21.2 x 50 5 868050-901PrepHT Endfittings, 2/pk 820400-901PrepHT Guard Cartridge, 2/pk 17.0 x 7.5 5 820212-928Guard Cartridge Hardware 820444-901


Standard Columns (no special hardware required)Hardware Description Size (mm)

Particle Size(µm)

Bonus-RPUSP L60

ZORBAX Bonus-RP



ZORBAX Original Reversed-Phase ColumnsAgilent Original ZORBAX columns are made with Type A silica and are useful for many applications of acidic or neutral compounds. These columns have ahigher activity level and are therefore useful for separating isomers (e.g. cis-trans, geometric) or other compounds where silanol activity enhances selectivity.These columns are used in many established methods.

ZORBAX Original Reversed-Phase Columns


Size (µm)ODS (C18)USP L1

C8USP L7

PhenylUSP L11

CnUSP L10

tMSUSP L13

Standard Columns (no special hardware required)Semi-Preparative 9.4 x 250 5 880952-202 880952-206Analytical (Endcapped) 4.6 x 250 5 880952-702 880952-706 880952-712 884950-507 880952-710Analytical (Non-endcapped) 4.6 x 250 5 884950-543Analytical 4.6 x 150 5 883952-702 883952-706 883952-712 884950-526 883952-710Solvent Saver 3.0 x 250 5 880952-302Solvent Saver 3.0 x 150 5 883952-302

guard Columns (hardware required)Guard Cartridge, 2/pk 9.4 x 15 7 820675-115 820675-115 820675-115 820675-124Guard Cartridge, 4/pk 4.6 x 12.5 5 820950-902 820950-906 820950-912 820950-905 820950-924Guard Hardware Kit 840140-901 840140-901 840140-901 840140-901 840140-901Guard Hardware Kit 820999-901 820999-901 820999-901 820999-901 820999-901

PrepHt Cartridge Columns (require endfittings kit 820400-901)PrepHT Cartridge 21.2 x 250 7 877952-102 877952-106 877952-105PrepHT Endfittings, 2/pk 820400-901 820400-901 820400-901


Bonded Phase Pore Size Surface Area temp Limit pH Range Endcapped Carbon LoadZORBAX C18 70Å 300 m2/g 60 °C 2.0 - 8.0 Yes/No 20%ZORBAX C8 70Å 300 m2/g 60 °C 2.0 - 8.0 Yes 12%ZORBAX-Phenyl 70Å 300 m2/g 60 °C 2.0 - 8.0 Yes 12%ZORBAX CN 70Å 300 m2/g 60 °C 2.0 - 8.0 N/A 7%ZORBAX-TMS 70Å 300 m2/g 60 °C 2.0 - 7.0 N/A 4%

284


Kits for Analytical HPLCZORBAX Method Development KitsAgilent offers a series of kits that allow for fast method development at an attractive price. Each kit contains3 columns. Six new kits have been added and are recommended for use with the new Agilent AutomatedMethod Development LC. Several of these kits contain Rapid Resolution HT (1.8 µm) columns in a variety of bonded phases for easy method optimization and several kits contain Rapid Resolution (3.5 µm) columnsin the same variety of bonded phases. These kits contain some of the Eclipse Plus family of columns forexcellent peak shape and optimum performance with a wide variety of compounds.

ZORBAX Method Development KitsRecommended for use with the Agilent Automated Method Development LC SystemDescription Part no.Rapid Resolution HT (RRHT) Selectivity Method Development Kit, 2.1 mm idIncludes 2.1 x 50 mm, 1.8 µm, 600 bar columns: one each Eclipse Plus C18, Eclipse Plus Phenyl-Hexyl and Bonus-RP

5190-1431

Rapid Resolution HT (RRHT) pH Method Development Kit, 2.1 mm idIncludes 2.1 x 50 mm, 1.8 µm, 600 bar columns: one each Eclipse Plus C18, SB-C18 and Extend-C18

5190-1432

Rapid Resolution HT (RRHT) Selectivity Method Development Kit, 4.6 mm idIncludes 4.6 x 50 mm, 1.8 µm, 600 bar columns: one each Eclipse Plus C18, Eclipse Plus Phenyl-Hexyl and Bonus-RP

5190-1433

Rapid Resolution HT (RRHT) pH Method Development Kit, 4.6 mm idIncludes 4.6 x 50 mm, 1.8 µm, 600 bar columns: one each Eclipse Plus C18, SB-C18 and Extend-C18

5190-1434

Rapid Resolution Selectivity Method Development Kit, 4.6 mm idIncludes 4.6 x 100 mm, 3.5 µm columns: one each Eclipse Plus C18, Eclipse Plus Phenyl-Hexyl and Bonus-RP

5190-1435

Rapid Resolution pH Method Development Kit, 4.6 mm idIncludes 4.6 x 100 mm, 3.5 µm columns: one each Eclipse Plus C18, SB-C18 and Extend-C18

5190-1436

ZORBAX Method Development Kits



ZORBAX Method Development KitsDescription Part no.StableBond Method Development KitIncludes 4.6 x 150 mm, 5 µm columns; one each: SB-C18, SB-CN and SB-Phenyl phases

5183-4624

Fast StableBond Method Development KitIncludes 4.6 x 75 mm, 3.5 µm columns; one each: SB-C18, SB-CN and SB-Phenyl phases

5183-4625

Eclipse XDB Method Development KitIncludes 4.6 x 150 mm, 5 µm columns; one each: XDB-C18, XDB-C8, XDB-Phenyl phases

5183-4626

Fast Eclipse XDB Method Development KitIncludes 4.6 x 75 mm, 3.5 µm columns; one each: XDB-C18, XDB-C8 and XDB-Phenyl phases

5183-4627

pH Method Development KitIncludes 4.6 x 150 mm, 5 µm columns; one each: SB-C18, XDB-C18 and Extend-C18 phases

5185-5807

Fast pH Method Development KitIncludes 4.6 x 75 mm, 3.5 µm columns; one each: SB-C18, XDB-C18 and Extend-C18 phases

5185-5808

Aqueous Method Development KitIncludes 4.6 x 150 mm, 5 µm columns; one each: SB-Aq, Bonus RP and SB-C18

5185-5809

Fast Aqueous Method Development KitIncludes 4.6 x 75 mm, 3.5 µm columns; one each: SB-Aq, Bonus RP and SB-C18

5185-5810

ZORBAX Cartridge Column Starter KitsHardware Description Part no.

ZORBAX C18 KitIncludes one 4.6 x 150 mm, 5 µm Eclipse XDB-C18 column; one 4.6 x 150 mm, 5 µm StableBond C18 column; cartridge holder;mounting tool; replacement filter (2/pk); and open-end wrench

5183-2021

ZORBAX C8 KitIncludes one 4.6 x 150 mm, 5 µm Eclipse XDB-C8 column; one 4.6 x 150 mm, 5 µm StableBond C8 column; cartridge holder;mounting tool; replacement filter (2/pk); and open-end wrench

5183-2022

286


ZORBAX Method Validation KitsZORBAX Method Validation Kits are supplied to customers who need the same HPLC column type (bondedphase, particle size, configuration) but from different manufacturing lots. To request columns from differentlots, contact Agilent Technologies or your local Agilent Authorized Distributor using the following procedure:

• Request Validation Kits (columns from different lots) by using Part Number 899999-888

• Indicate the Part Number of the current column you are using

• Indicate the Lot Number of the current column you are using

• Indicate the number of additional columns needed from different lots (example: you have a current column and may need two additional lots)

• Please fax your request to (302) 993-5354 (United States and Canada) or email to [email protected]. You will receive a quote from your Customer Service Representative within 1-2 business days. Delivery of your method validation kit is usually 3 weeks or less from the time your order is placed, depending on lot availability.

Custom HPLC Column OrderingColumns not listed can be easily ordered using the following procedure:

• Request a Special Products Quotation (SPQ) using Part Number 899999-999

• Indicate column dimensions (example: 4.6 x 50 mm); bonded phase type (example: StableBond C3);particle size (example: 5 µm); and pore size (example: 80Å)

• Please fax your request to (302) 993-5354 (United States and Canada) or email to [email protected]. You will receive a quote from your Customer Service Representative within 1-2 business days. Delivery of your custom column is usually 3 weeks or less from the time your order is placed, depending on lot availability.

Custom columns are priced with a minimal surcharge over the price of stocked columns.



Pursuit HPLC ColumnsBeginning in drug discovery and drug metabolism, Pursuit columns are ideal for analyzing lead compoundsand biological samples. The column's performance is due to the unique combination of advanced bondingchemistry and ultra-high purity silica. These factors combine to provide rapid separations with excellent firsttime resolution and symmetrical peaks for polar compounds, whether at pH 1.5 or 10. Additionally, the needfor ion-pairing agents such as TFA is often eliminated, thus maximizing the performance of single andparallel multi-channel LC/MS systems.

Culminating in QC, Pursuit is ideal for implementing dependable trouble-free analysis of raw materials andapproved drugs. Rigorous control and validation of each step in the manufacturing process ensures columnreproducibility. With Pursuit, your laboratory can spend its energy on producing results.

Special columns, such as Pursuit PFP (for very polar compounds) and Pursuit PAH (environmental), give youthe extra selectivities you need for your most challenging applications.

Pursuit

Pursuit XRs

Pursuit XRs UltraFor the ultimate in speed and good resolution on any instrument, we designed the Pursuit XRs Ultra aroundan optimized 2.8 µm particle and an advanced packing procedure. Now you can decrease your run timewhile maintaining resolution. Lower backpressure allows high flow rates to be used, and the 2.8 µmparticles of ultra-pure silica delivers 10-15% higher efficiency than 3 µm columns.

For LC/MS and high throughput applications, the Pursuit column is built on the larger 200Å pore size silica.High ligand density delivers up to 40% faster separations without sacrificing resolution. This is accomplishedby optimizing mass transfer with the larger pore size.

Pursuit XRs columns are for performance in analytical R&D, QC and preparative applications. Combininghigh ligand density with a 100Å pore size, high surface area silica, Pursuit XRs columns are designed toincrease productivity, as they offer maximum loadability, excellent stability and easy scalability whilemaintaining superior resolution.

Pursuit HPLC Columns

288


tiPS & tOOLS

Request custom LC columns online at www.agilent.com/chem/customlccol


Bonded Phase Pore Size Surface Area pH Range EndcappedCarbonLoad Pore Volume Ligand Coverage

Pursuit C18 200Å 200 m2/g 1.5-10 Yes 12.9% 11 mL/g 3.5 µmol/m2

Pursuit C8 200Å 200 m2/g 1.5-10 Yes 7.4% 11 mL/g 3.8 µmol/m2

Pursuit Diphenyl 200Å 200 m2/g 1.5-8.0 Yes 7.3% 11 mL/g 2.8 µmol/m2

Pursuit PFP 200Å 200 m2/g 1.5-10 Yes 6.3% 11 mL/g 3.4 µmol/m2

Pursuit PAH 200Å 200 m2/g 1.5-10 Yes 11 mL/gPursuit XRs C18 100Å 440 m2/g 1.5-10 Yes 22% 11 mL/g 2.9 µmol/m2

Pursuit XRs C8 100Å 440 m2/g 1.5-10 Yes 15% 11 mL/g 3.7 µmol/m2

Pursuit XRs Diphenyl 100Å 440 m2/g 1.5-8.0 Yes 14.6% 11 mL/g 2.6 µmol/m2

Pursuit XRs Si 100Å 440 m2/g 1.5-10 Yes 11 mL/gPursuit XRs Ultra C18 100Å 440 m2/g 1.5-10 Yes 23.2% 11 mL/g 3.2 µmol/m2

Pursuit XRs Ultra C8 100Å 440 m2/g 1.5-10 Yes 15% 11 mL/g 3.7 µmol/m2

Pursuit XRs Ultra Diphenyl 100Å 440 m2/g 1.5-8.0 Yes 14.6% 11 mL/g 2.6 µmol/m2

Specifications represent typical values only

1 23

1 23

0

0

mA

U

400

VLC0002min 6

0

0

mA

U

400

min 6



12

34

56 7

89 10

11 12 13 14

0

0

mAU

24

VLC0001min 24

tricyclic antidepressants and benzodiazepinesColumn: Pursuit XRs C18

A6000150X0464.6 x 150 mm, 5 µm

Mobile Phase: A: Water+0.1% HCOOHB: MeCN+0.1% HCOOH

Gradient: 30-40% B in 15 min, hold at 40% B for 15 min




1. 7-Aminoclonazepam2. 7-Aminoflunitrazepam3. Nordoxepin4. Doxepin5. Desipramine6. Imipramine7. Nortriptyline8. Amitriptyline9. Trimipramine

10. Clomipramine11. Nordiazepam12. Clonazepam13. Flunitrazepam14. Diazepam

Mechanical stability of Pursuit XRsColumn: Pursuit XRs C18

A6000050X0202.0 x 50 mm, 5 µm

Sample: DMSO mix

Mobile Phase: A: MeOH:water, 10:90 + 0.1% HCOOHB: MeOH:water, 90:10 + 0.1% HCOOH

Gradient: 0-100% B in 3 min, back to 0% B in 0.5 min, hold at0% B for 3.5 min




1. 4-Methoxybenzenesulfonamide2. Methyl 3-aminothiophene-2-carboxylate3. Trimipramine

injection 5000

injection 1

290


1

2

3

4

0

0

µV

240,000

VLC0003

min 6

Pursuit PfP1. Triamcinolone2. Prednisolone3. Cortisone4. Methylprednisolone5. Corticosterone6. Beclomethasone7. Prednisolone acetate8. Triamcinolone acetonide9. Cortisone acetate

10. Fluocinolone acetonide

Adrenocorticosteroids on Pursuit PfP and C18Mobile Phase: MeCN:water, 22.5:77.5




Liquid chromatography phase test mixture(LPtM) on Pursuit C8Column: Pursuit C8

A3031050X0202.0 x 50 mm, 3 µm

Mobile Phase: A: 0.05% HCOOH in waterB: 0.05% HCOOH in MeCN



AntifungalsColumn: Pursuit XRs Ultra Diphenyl

A7521050X0202.0 x 50 mm, 2.8 µm

Mobile Phase: Water+0.1% HCOOH:MeCN+0.1% HCOOH, 80:20




1. 4-Aminobenzoic acid2. Sorbic acid3. Benzoic acid4. Salicylic acid

1. Aspartame2. Cortisone3. Reserpine4. Dioctyl phthalate

12

3

45 6 7 8

10

9

1 23

45 6 7 8

109

VLC0005

0

0

300

mA

U

min 25

0

0

300

mA

U

min 25

1

23

4

2 VLC0004min 5

Pursuit C18



Pursuit HPLC ColumnsSemi-Prep Scale

Size (mm) Particle Size (µm)Pursuit C18USP L1

Pursuit C8USP L7 Pursuit Diphenyl Pursuit PfP

Pursuit PAHUSP L1

10.0 x 250 10 A3002250X100 A3032250X10010.0 x 150 5 A3000150X100 A3050150X10010.0 x 250 5 A3000250X100 A3030250X100 A3050250X100

(Continued)

Pursuit HPLC ColumnsAnalytical Scale



Pursuit PAHUSP L1

4.6 x 250 10 A3002250X046 A3032250X0464.6 x 150 10 A3002150X046 A3032150X0464.6 x 100 10 A3002100X046 A3032100X0464.6 x 250 5 A3000250X046 A3030250X046 A3040250X046 A3050250X046 A7000250X0464.6 x 150 5 A3000150X046 A3030150X046 A3040150X046 A3050150X046 A7000150X0464.6 x 100 5 A3000100X046 A3030100X046 A3040100X046 A3050100X0464.6 x 50 5 A3000050X046 A3030150X046 A3040050X046 A3050050X0464.6 x 250 3 A3001250X046 A3031250X046 A3041250X046 A3051250X0464.6 x 150 3 A3001150X046 A3031150X046 A3041150X046 A3051150X0464.6 x 100 3 A3001100X046 A3031100X046 A3041100X046 A3051100X046 A7001100X0464.6 x 50 3 A3001050X046 A3041050X046 A3051050X0464.6 x 30 3 A3001030X0464.0 x 250 5 A3000250X0404.0 x 125 5 A3000125X0403.9 x 300 10 A3002300X0393.9 x 300 5 A3000300X0393.9 x 150 5 A3000150X0393.0 x 250 5 A3000250X030 A3040250X0303.0 x 150 5 A3000150X030 A3040150X030 A3050150X0303.0 x 100 5 A3000100X030 A3050100X0303.0 x 250 3 A3001250X0303.0 x 150 3 A3001150X030 A3041150X030 A3051150X0303.0 x 100 3 A3001100X030 A3041100X030 A3051100X030 A7001100X030

292


Pursuit HPLC ColumnsPrep Scale



Pursuit PAHUSP L1

50.0 x 250 10 A3002250X500 A3032250X50021.2 x 250 10 A3002250X212 A3032250X21221.2 x 150 10 A3002150X21221.2 x 250 5 A3000250X212 A3050250X21221.2 x 150 5 A3000150X212 A3050150X21221.2 x 100 5 A3040100X212

3.0 x 50 3 A3001050X030 A3041050X030 A3051050X0302.0 x 250 5 A3000250X0202.0 x 150 5 A3000150X020 A3030150X020 A3040150X0202.0 x 100 5 A3000100X020 A3030100X020 A3040100X020 A3050100X0202.0 x 50 5 A3000050X020 A3030050X020 A3040050X020 A3050050X0202.0 x 30 5 A3000030X020 A3040030X020 A3050030X0202.0 x 20 5 A3000020X020 A3050020X0202.0 x 250 3 A3001250X020 A3041250X0202.0 x 200 3 A3041200X0202.0 x 150 3 A3001150X020 A3031150X020 A3041150X020 A3051150X0202.0 x 100 3 A3001100X020 A3031100X020 A3041100X020 A3051100X020 A7001100X0202.0 x 50 3 A3001050X020 A3031050X020 A3041050X020 A3051050X0202.0 x 30 3 A3001030X020 A3031030X020 A3041030X020 A3051030X0202.0 x 20 3 A3001020X020 A3041020X020 A3051020X020



Pursuit PAHUSP L1

Analytical Scale

Pursuit HPLC Columns



Pursuit ChromSep Complete Cartridge Systems

Hardware Size (mm) Particle Size (µm)Pursuit C18USP L1

Pursuit C8USP L7

Pursuit PAHUSP L1

4.6 x 250 5 A3000250C046 A3030250C046 A7000250C0464.6 x 250 3 A3031250C0464.6 x 150 5 A3000150C046 A3030150C046 A7000150C0464.6 x 100 5 A3000100C046 A3030100C0464.6 x 150 3 A3001150C046 A3031150C046 A7001150C0464.6 x 100 3 A3001100C046 A3031100C046 A7001100C0464.6 x 50 3 A3001050C0463.0 x 250 5 A3000250C0303.0 x 150 5 A3000150C0303.0 x 100 5 A3000100C030 A7000100C0303.0 x 150 3 A3001150C0303.0 x 100 3 A3001100C0302.0 x 250 5 A3000250C0202.0 x 150 5 A3000150C020 A3030150C0202.0 x 100 5 A3000100C0202.0 x 150 3 A3001150C0202.0 x 100 3 A3001100C0202.0 x 50 3 A3001050C020

294


Pursuit ChromSep Replacement Cartridges

Hardware Size (mm) Particle Size (µm) UnitPursuit C18USP L1

Pursuit C8USP L7

Pursuit PAHUSP L1

4.6 x 250 5 A7000250R0463/pk A7000250T046

4.6 x 150 5 A3000150R046 A3030150R046 A7000150R0463/pk A3000150T046 A3030150T046 A7000150T046

4.6 x 150 3 A3031150R046 A7001150R0463/pk A3031150T046 A7001150T046

4.6 x 100 3 A7001100R0463/pk A7001100T046

4.6 x 50 3 A3001050R0463/pk A3001050T046

3.0 x 150 5 A3000150R0303/pk A3000150T030

3.0 x 100 5 A3000100R030 A7000100R0303/pk A3000100T030 A7000100T030

3.0 x 150 3 A3001150R0303/pk A3001150T030

3.0 x 100 3 A3001100R030 A7001100R0303/pk A3001100T030 A7001100T030

2.0 x 50 3 A3031050R0203/pk A3031050T020

Metaguard Columns, 3/pkHardware iD (mm) Particle Size (µm) Pursuit C18 Pursuit C8 Pursuit DP Pursuit PfP

4.6 10 A3002MG2.0 10 A3002MG24.6 5 A3000MG A3030MG A3040MG A3050MG2.0 5 A3000MG2 A3030MG2 A3040MG2 A3050MG21.0 5 A3000MG1 A3040MG14.6 3 A3001MG A3031MG A3041MG A3051MG2.0 3 A3001MG2 A3031MG2 A3041MG2 A3051MG21.0 3 A3041MG1



(Continued)

Pursuit XRs HPLC ColumnsSemi-Prep Scale

Size (mm)Particle Size

(µm)

PursuitXRs C18USP L1

Pursuit XRs C8USP L7

PursuitXRs DiphenylUSP L11

PursuitXRs Si*USP L3

10.0 x 250 10 A6002250X100 A6004250X10010.0 x 250 5 A6000250X100 A6020250X10010.0 x 150 5 A6000150X10010.0 x 50 5 A6000050X10010.0 x 150 3 A6021150X100*Pursuit XRs Si is a normal phase column.

Pursuit XRs HPLC ColumnsAnalytical Scale


(µm)





4.6 x 250 10 A6002250X046 A6004250X0464.6 x 50 10 A6002050X046S4.6 x 250 5 A6000250X046 A6010250X046 A6020250X0464.6 x 150 5 A6000150X046 A6010150X046 A6020150X0464.6 x 100 5 A6000100X046 A6010100X046 A6020100X046 A6006100X0464.6 x 50 5 A6000050X046 A6020050X046 A6006050X0464.6 x 250 3 A6001250X046 A6021250X0464.6 x 150 3 A6001150X046 A6010150X046 A6021150X0464.6 x 100 3 A6001100X046 A6011100X046 A6021100X046 A6005100X0464.6 x 50 3 A6001050X046 A6011050X046 A6021050X046 A6005050X0464.6 x 30 3 A6001030X046 A6021030X0464.0 x 250 5 A6000250X040 A6010250X0404.0 x 150 5 A6000150X040 A6010150X0403.0 x 250 5 A6000250X030 A6010250X030 A6020250X0303.0 x 150 5 A6000150X030 A6010150X030 A6020150X0303.0 x 100 5 A6000100X030 A6010100X030 A6020100X0303.0 x 150 3 A6001150X030 A6011150X030 A6021150X0303.0 x 100 3 A6001100X030 A6011100X030 A6021100X0303.0 x 50 3 A6001050X030 A6011050X030 A6021050X0303.0 x 30 3 A6001030X030*Pursuit XRs Si is a normal phase column.

296


2.1 x 100 5 A6006100X0212.0 x 250 5 A6000250X020 A6020250X0202.0 x 150 5 A6000150X020 A6010150X020 A6020150X0202.0 x 100 5 A6000100X020 A6010100X0202.0 x 50 5 A6000050X020 A6010050X020 A6020050X0202.0 x 30 5 A6000030X0202.0 x 250 3 A6001250X020 A6021250X0202.0 x 150 3 A6001150X020 A6011150X020 A6021150X0202.0 x 100 3 A6001100X020 A6011100X020 A6021100X0202.0 x 50 3 A6001050X020 A6011050X020 A6021050X020 A6005050X0202.0 x 30 3 A6021030X0202.0 x 20 3 A6001020X0201.0 x 150 3 A6001150X0101.0 x 100 3 A6001100X010 A6021100X010*Pursuit XRs Si is a normal phase column.


(µm)





Analytical Scale

Pursuit XRs HPLC Columns

Pursuit XRs HPLC ColumnsPrep Scale


(µm)





50.0 x 250 10 A6002250X500 A6002250X500 A6004250X50030.0 x 250 5 A6000250X300 A6004250X30030.0 x 150 5 A6000150X300 A6020150X30030.0 x 100 5 A6000100X30030.0 x 50 5 A6000050X30021.2 x 250 10 A6002250X212 A6012250X212 A6004250X21221.2 x 250 5 A6000250X212 A6020250X21221.2 x 150 5 A6000150X21221.2 x 100 5 A6000100X212 A6020100X21221.2 x 50 5 A6000050X21221.2 x 30 5 A6000030X212*Pursuit XRs Si is a normal phase column.



Pursuit XRs Ultra HPLC Columns


(µm)Pursuit XRs Ultra C18

Pursuit XRs Ultra C8

Pursuit XRs Ultra Diphenyl

3.0 x 150 2.8 A7501150X030 A7511150X0303.0 x 100 2.8 A7501100X0302.0 x 150 2.8 A7501150X0202.0 x 100 2.8 A7501100X020 A7511100X020 A7521100X0202.0 x 50 2.8 A7501050X020 A7511050X020 A7521050X0202.0 x 30 2.8 A7501030X020 A7511030X020 A7521030X020

Metaguard Columns, 3/pk

Hardware iD (mm) Particle Size (µm) Pursuit XRs C18 Pursuit XRs Si Pursuit XRs C8Pursuit XRsDiphenyl Pursuit PAH

4.6 10 A6002MG A6004MG4.6 5 A6000MG A6010MG A6020MG3.0 5 A7000MG32.0 5 A6000MG2 A6010MG2 A6020MG24.6 3 A6001MG A6011MG A6021MG3.0 3 A7001MG32.0 3 A6001MG2 A6011MG2 A6021MG2 A6001MG2

298


Polaris HPLC ColumnsIn areas like drug discovery where target compounds are increasingly polar, it is critical to have a reversed-phase column that performs well under aqueous conditions. Retention is critical, but cannot come with troublesome secondary interactions. Likewise, phase collapse and shifting retention times need to be avoided. The answer is our Polaris line of polar-modified columns.

From the collapse-resistant pore structure of our base silica, to the "wettability" engineered into the bonded phases, Polaris columns have been designed for high aqueous conditions. The combination of high phase density bonding, ultra pure silica, and silanol shielding leads to excellent peak shape amongpolar-modified columns.

As a family, Polaris offers a variety of polar modifications in both C18 and C8 chemistries.

Polaris C18-APolaris C18-A is the best starting place for separations where the benefits of polar-modified columns are desired. The polar modifications of C18-A help it avoid poor peak shape and retention issues in loworganic conditions.

Polaris C8-APolaris C8-A offers an alternative selectivity to standard C8 phases and has a lower hydrophobicity thanPolaris C18-A, making it ideal for polar samples, or faster overall analysis times.

Polaris C18-EtherPolaris C18-Ether offers an alternative selectivity to Polaris C18-A and standard C18 phases, and typicallydelivers increased retention of polar compounds away from the void volume.

Polaris C8-EtherPolaris C8-Ether offers an alternative selectivity to Polaris C8-A with particular utility for hydrogen bonding compounds.


Bonded Phase Pore SizeSurface

AreaCarbonLoad Endcapped

PoreVolume Ligand Coverage

Polaris C18-A 180Å 200 m2/g 13.8% Yes 1.1 cm3/g 3.9 µmol/m2

Polaris C8-A 180Å 200 m2/g 7.4% Yes 1.1 cm3/g 4.8 µmol/m2

Polaris C18-Ether 180Å 200 m2/g 12.1% Yes 1.1 cm3/g 3.3 µmol/m2

Polaris C8-Ether 180Å 200 m2/g 7.1% Yes 1.1 cm3/g 4.5 µmol/m2

Polaris Amide C18 180Å 200 m2/g 15% Yes 1.1 cm3/g 4.4 µmol/m2

Polaris NH2 180Å 200 m2/g 5.5% Amide 1.1 cm3/g 3.8 µmol/m2

Polaris Si-A 180Å 200 m2/g N/A N/A 1.1 cm3/g N/A


Polaris HPLC Columns



Selectivity test mix for Polaris columnsMobile Phase: MeCN:water 70:30




12 3 4

5

6

7

8

1 2 3 4

5+8

6

7

VLC00070

0

400

mA

Umin 14

0

0

400

mA

U

min 14

Polaris C8-A

Polaris C18-A

1. Uracil2. Caffeine3. Phenol4. Toluene5. Butylbenzene6. o-Terphenyl7. Amylbenzene8. Triphenylene

LC/MS performance test mix for Polaris C8-AColumn: Polaris C8-A

A2011030X0303.0 x 30 mm, 3 µm

Mobile Phase: A: Water+0.05% HCOOHB: MeCN+0.05% HCOOH

Gradient: 5-90% B in 3 min and hold for 4 min




1

2

34

VLC00080

0

400

mA

U

min 8

1. Aspartame2. Cortisone3. Reserpine4. Dioctyl phthalate

300



Size (mm)Particle

Size (µm)PolarisC18-A

PolarisC8-A

PolarisC18-Ether

PolarisC8-Ether

Polaris Amide C18

PolarisnH2*

PolarisSi-A*

50.0 x 250 10 A2002250X500 A2004250X50030.0 x 100 5 A2000100X30030.0 x 3.0 3 A2007030X03021.2 x 250 10 A2002250X212 A2008250X212 A2004250X21221.2 x 250 5 A2000250X212 A2010250X212 A2020250X212 A2030250X212 A2006250X212 A2013250X212 A2003250X21221.2 x 150 5 A2000150X212 A2003150X04621.2 x 100 5 A2000100X21221.2 x 50 5 A2003050X21210.0 x 250 10 A2008250X10010.0 x 250 5 A2000250X100 A2020250X100 A2030250X100 A2006250X100 A2013250X10010.0 x 50 3 A2021050X1004.6 x 250 10 A2002250X046 A2003250X0464.6 x 250 5 A2000250X046 A2010250X046 A2020250X046 A2030250X046 A2006250X046 A2013250X0464.6 x 200 5 A2000200X0464.6 x 150 5 A2000150X046 A2010150X046 A2020150X046 A2030150X046 A2006150X046 A2013150X046 A2003150X0464.6 x 100 5 A2000100X046 A2010100X046 A2006100X046 A2013100X046 A2003100X0464.6 x 50 5 A2000050X046 A2020050X046 A2006050X046 A2013050X046 A2003050X0464.6 x 30 5 A2000030X0464.6 x 250 3 A2001250X046 A2021250X046 A2031250X046 A2007250X046 A2014250X046 A2005250X0464.6 x 150 3 A2001150X046 A2011150X046 A2007150X046 A2014150X046 A2005150X0464.6 x 100 3 A2001100X046 A2011100X046 A2007100X046 A2014100X046 A2005100X0464.6 x 75 3 A2001075X046 A2011075X046*Normal phase columns.

(Continued)



4.6 x 50 3 A2001050X046 A2021050X046 A2031050X046 A2007050X046 A2014050X046 A2005050X0464.6 x 30 3 A2001030X0464.0 x 250 5 A2000250X040 A2010250X040 A2020250X040 A2030250X040 A2013250X040 A2003250X0404.0 x 150 5 A2000150X040 A2010150X040 A2020150X040 A2030150X040 A2013150X040 A2003150X0404.0 x 125 5 A2000125X040 A2010125X040 A2020125X040 A2030125X040 A2013125X040 A2003125X0403.0 x 250 5 A2000250X030 A2010250X030 A2020250X030 A2030250X030 A2006250X030 A2013250X030 A2005250X0463.0 x 150 5 A2000150X030 A2010150X030 A2020150X030 A2030150X030 A2006150X030 A2013150X030 A2003150X0303.0 x 100 5 A2000100X030 A2010100X030 A2020100X030 A2030100X030 A2006100X030 A2013100X030 A2003100X0303.0 x 50 5 A2000050X030 A2003050X0303.0 x 250 3 A2001250X030 A2007250X030 A2014250X030 A2003250X0303.0 x 200 3 A2001200X0303.0 x 150 3 A2001150X030 A2021150X030 A2007150X030 A2014150X030 A2005150X0303.0 x 100 3 A2001100X030 A2007100X030 A2014100X030 A2005100X0303.0 x 50 3 A2001050X030 A2021050X030 A2031050X030 A2007050X030 A2014050X030 A2005050X0303.0 x 30 3 A2001030X030 A2011030X0302.0 x 250 5 A2000250X020 A2020250X020 A2030250X020 A2006250X020 A2013250X020 A2003250X0202.0 x 150 5 A2000150X020 A2010150X020 A2020150X020 A2030150X020 A2006150X020 A2013150X020 A2003150X0202.0 x 100 5 A2000100X020 A2006100X020 A2013100X020 A2003100X0202.0 x 50 5 A2000050X020 A2010050X020 A2020050X020 A2030050X020 A2006050X020 A2013050X020 A2003050X0202.0 x 30 5 A2000030X020 A2006030X020 A2013030X020 A2003030X0202.0 x 20 5 A2000020X020 A2013020X020 A2003020X0202.0 x 250 3 A2001250X020 A2011250X020 A2021250X020 A2031250X020 A2007250X020 A2014250X020 A2005250X0202.0 x 150 3 A2001150X020 A2011150X020 A2021150X020 A2031150X020 A2007150X020 A2014150X020 A2005150X0202.0 x 100 3 A2001100X020 A2021100X020 A2031100X020 A2007100X020 A2014100X020 A2005100X0202.0 x 75 3 A2021075X0202.0 x 50 3 A2001050X020 A2011050X020 A2021050X020 A2031050X020 A2007050X020 A2014050X020 A2005050X020


Size (mm)Particle

Size (µm)PolarisC18-A

PolarisC8-A

PolarisC18-Ether

PolarisC8-Ether

Polaris Amide C18

PolarisnH2*

PolarisSi-A*

2.0 x 30 3 A2001030X020 A2021050X020 A2007030X020 A2014030X020 A2005030X0202.0 x 20 3 A2001020X020 A2014020X020 A2005020X020*Normal phase columns.

302


Polaris ChromSep Complete Cartridge Systems

Hardware Size (mm) Particle Size (µm)PolarisC18-A

4.6 x 250 5 A2000250C0464.6 x 150 5 A2000150C0464.6 x 100 5 A2000100C0464.6 x 250 3 A2001250C0464.6 x 150 3 A2001150C0463.0 x 250 5 A2000250C0303.0 x 100 5 A2000100C0302.0 x 100 5 A2000100C0202.0 x 150 3 A2001150C0202.0 x 100 3 A2001100C0202.0 x 50 3 A2001050C020

Polaris ChromSep Replacement Cartridges

Hardware Size (mm) Particle Size (µm) UnitPolarisC18-A

4.6 x 250 5A2000250R046

3/pk A2000250T046

4.6 x 150 5A2000150R046

3/pk A2000150T046

4.6 x 100 5A2000100R046

3/pk A2000100T046

4.6 x 150 3A2001150R046

3/pk A2001150T046

4.6 x 100 3A2001100R046

3/pk A2001100T046

3.0 x 150 5A2000150R030

3/pk A2000150T030

3.0 x 100 5A2000100R030

3/pk A2000100T030

3.0 x 100 3A2001100R030

3/pk A2001100T030

2.0 x 150 3A2001150R020

3/pk A2001150T020

2.0 x 50 3A2001050R020

3/pk A2001050T020



Metaguard Columns

Hardware Dimensions

ParticleSize(µm)

PolarisC18-A

Polaris C8-A

PolarisC18-Ether

Polaris C8-Ether

PolarisAmide C18

PolarisnH2*

Polaris Si-A*

4.6 10 A2002MG A2004MG2.0 10 A2008MG2 A2004MG24.6 5 A2000MG A2010MG A2020MG A2030MG A2006MG A2013MG A2003MG2.0 5 A2000MG2 A2010MG2 A2020MG2 A2006MG2 A2013MG2 A2003MG24.6 3 A2001MG A2011MG A2021MG A2007MG A2014MG A2005MG2.0 3 A2011MG2 A2011MG2 A2021MG2 A2031MG2 A2007MG2 A2014MG2 A2005MG21.0 3 A2001MG1

*Normal phase columns.

304


Agilent tC-C18(2) and HC-C18(2)For cost-conscious chromatographers who need traditional LC columns and don't need the individual testing of ZORBAX, Pursuit or Polaris columns, the Agilent TC(2)/HC(2) columns provide an alternative.

TC-C18(2)Agilent TC-C18(2) is the ideal choice for complex natural product extract samples, traditional medicines and environmental samples or any sample where you need to analyze mixtures of polar and non-polarcompounds, including strong basic compounds.

• Lower carbon load – 12%• Ideal for polar compounds and gradient separations that start at low % organic or cover a wide

organic range• Good choice for samples dissolved in water, or mostly water• Use with most common mobile phases, including formic acid, acetic acid, trifluoroacetic acid (TFA)

and phosphate buffers with acetonitrile and methanol as the organic modifiers• Excellent performance from pH 2-8

HC-C18(2)Agilent HC-C18(2) is a more retentive C18 with a higher carbon load. An excellent value alternative to other high carbon load columns, it also provides superior peak shape for basic compounds.

• Higher carbon load – 17% – provides greater retention for moderately polar and non-polar compounds

• Ideal for non-polar compounds and separations that start at mid-level % organic (at least greater than 10% organic)

• Good choice for industrial samples or samples dissolved in organic/mostly organic solvents• Stable over a very wide pH range (2-9) for maximum flexibility



Agilent HC-C18(2) and tC-C18(2)Description Size (mm) Particle Size (µm) Part no.Agilent HC-C18(2) 4.6 x 250 5 588905-902Agilent HC-C18(2) 4.6 x 150 5 588915-902Agilent TC-C18(2) 4.6 x 250 5 588925-902Agilent TC-C18(2) 4.6 x 150 5 588935-902Agilent HC-C18(2) guards, 2/pk 4.6 x 12.5 5 520518-904Agilent TC-C18(2) guards, 2/pk 4.6 x 12.5 5 520518-905Guard Hardware Kit 820999-901

tiPS & tOOLS


BondedPhase Pore Size Surface Area

temp.Limits pH Range* Endcapped

CarbonLoad

TC-C18(2) 170Å 290 m2/g 60 °C 2.0-8.0 Yes 12%HC-C18(2) 170Å 290 m2/g 60 °C 2.0-9.0 Yes 17%


Don't forget, we have special offers throughout the year.

To learn more, visit www.agilent.com/chem/specialoffers

306


PLRP-S HPLC Columns• Contain durable and resilient polymer particles that deliver reproducible results over longer lifetimes• Thermally and chemically stable• Comply with USP L21 designation• Used in bioscience, chemical, clinical research, energy, environmental, food and agriculture, material

science and pharmaceutical industries• Pore sizes (100Å-4000Å) for separations of small molecules to large complexes and polynucleotides


pH Range 1-14Buffer Content UnlimitedOrganic Modifier 1-100%Temperature Limits 200 °CMaximum Pressure 5-8 µm: 3000 psi (210 bar)

3 µm: 4000 psi (300 bar)

PLRP-S Applications

Pore Size Application100Å Small molecules/synthetic biomolecules 300Å Recombinant peptides/proteins1000Å Large proteins4000Å DNA/high speed

The PLRP-S family of columns consists of a range of pore sizes and particle sizes, all with identical chemistryand fundamental adsorptive characteristics. The particles are inherently hydrophobic, therefore no bondedphase, alkyl ligand is required for reversed-phase separations. This gives a highly reproducible material thatis free from silanols and heavy metal ions. Columns within the extensive product range are suitable for microseparations, including both bottom-up and top-down proteomics, analytical separations, and preparativepurifications. In addition, process columns can be packed with bulk media.



HPLC

PLRP-S 100Å

PLRP-S 300Å

PLRP-S 1000Å

PLRP-S 4000Å

Resp

onse

, UV,

260

nm

TimeVLCPLRPSResp

HPLC of 25 bp DnA ladder Column: PLRP-S, 2.1 x 150 mmMobile Phase: A: 0.1 M TEAA

B: 0.1 M TEAA in 50% water:50% ACN

Flow Rate: 200 µL/min

Gradient: 12.5-50% B in 150 min

Polyethylene glycolsColumn: PLRP-S 100Å

PL1111-35004.6 x 150 mm, 5 µm

Mobile Phase: A: WaterB: ACN

Gradient: 10-30% B in 12 min, held at 30% B for 3 min


Injection Volume: 10 µL

Sample Conc: 1 mg/mL

Detector: ELS (neb=50 °C, evap=70 °C, gas=1.6 SLM)

0

PEG 400

PEG 1080

VLC0048

15

0 15

min

min

308


0

1 mM

10 mM

100 mM

VLC0049

10 min

1

2

3

1. Angiotensin II2. Angiotensin I3. Angiotensin III

Exploiting chemical stability – nH4OH concentrationColumn: PLRP-S 100Å

PL1512-55004.6 x 250 mm, 5 µm

Mobile Phase: A: NH4OH (various mM) in waterB: NH4OH (various mM) in ACN

Gradient: Linear 10-100% B in 15 min



0

4

5

VLC0050

30min

12

3

Alberta Peptide institute test mixColumn: PLRP-S 100Å

PL1512-55004.6 x 250 mm, 5 µm

Mobile Phase: A: 0.1% TFA in 99% water:1% ACNB: 0.1% TFA in 70% water:30% ACN

Gradient: 0-100% B in 30 min



1. Ala3-Gly4 (free amino)2. Gly3-Gly4 (Na-acetylated)3. Ala3-Gly4 (Na-acetylated)4. Val3-Gly4 (Na-acetylated)5. Val3-Val4 (Na-acetylated)



0 12VLC0051

min 0 18min

1

PLRP-S 300Å PLRP-S 1000Å

2

1

2

1. Collagen (120,000 MW)2. Fibrinogen (340,000 MW)

Large fibrous proteinsColumn: PLRP-S 300Å

PL1512-38014.6 x 150 mm, 8 µm

Column: PLRP-S 1000ÅPL1512-38024.6 x 150 mm, 8 µm

Mobile Phase: A: 0.25% TFA in waterB: 0.25% TFA in 5% water:95% ACN




310


PLRP-S HPLC Columns

Hardware Size (mm) Particle Size (µm)

PLRP-S100ÅUSP L21

PLRP-S300ÅUSP L21

PLRP-S1000ÅUSP L21

PLRP-S4000ÅUSP L21

4.6 x 250 8 PL1512-5800 PL1512-5801 PL1512-58024.6 x 150 8 PL1512-3800 PL1512-3801 PL1512-3802 PL1512-38034.6 x 50 8 PL1512-1801 PL1512-1802 PL1512-18034.6 x 250 5 PL1512-5500 PL1512-55014.6 x 150 5 PL1111-3500 PL1512-35014.6 x 50 5 PL1512-1500 PL1512-1501 PL1512-1502 PL1512-15034.6 x 150 3 PL1512-3300 PL1512-33014.6 x 50 3 PL1512-1300 PL1512-13012.1 x 250 8 PL1912-58012.1 x 150 8 PL1912-3801 PL1912-3802 PL1912-38032.1 x 50 8 PL1912-1801 PL1912-1802 PL1912-18032.1 x 250 5 PL1912-5500 PL1912-55012.1 x 150 5 PL1912-3500 PL1912-35012.1 x 50 5 PL1912-1500 PL1912-1501 PL1912-1502 PL1912-15032.1 x 150 3 PL1912-3300 PL1912-33012.1 x 50 3 PL1912-1300 PL1912-1301PLRP-S Guard Cartridges for 5 x 3 mm, 2/pk PL1612-1801 PL1612-1801 PL1612-1801 PL1612-1801Guard Cartridge holder for 3.0 x 5.0 mm cartridges PL1310-0016 PL1310-0016 PL1310-0016 PL1310-0016

*Prep columns are also available for the PLRP-S family. Turn to pages 467-471

311www.agiLent.Com/CHem/LC

CoLumns for smaLL moLeCuLe seParations

Whether you are scaling up a routine analytical method, or maintaining precise separations throughoutevery phase of production, Agilent can help you rise to the challenge.

• High loadability for maximum sample purification• Easy scalability from 4.6 up to 50 mm id for rapid method development• High throughput 21.2 mm id cartridges for fast purification• Exceptional column stability and loadability up to pH 10

Agilent Prep LC columns are designed for high loadability to purify milligram to gram quantities of products.Preparative sized columns are available in 21.2, 30, and 50 mm internal diameters with lengths rangingfrom 50-250 mm. Columns are available in 5 and 10 µm particle sizes with very high efficiency in everydimension. These column choices accommodate almost every preparative sample.

Agilent Prep 21.2 mm id columns are available with Agilent’s Preparative Cartridge Hardware. This reliablecartridge hardware makes it simple to use columns with different lengths to increase sample load. Guardcolumns are easily integrated onto these columns, providing superior protection of the analysis column.Analytical size 4.6 mm id scalar columns are available for method development and optimization prior toscaling up to larger columns. Bulk material is also available.

Agilent Prep columns are available in a C18 bonded phase suitable for purification of a wide variety of non-polar and polar compounds. Unbonded silica columns are also available.

Flexible, cost-effective options for scaling and prep

Agilent Prep LC Columns

• Agilent Prep LC columns are a cost-effective prep solution designed for high loadability to purifymilligram to gram quantities of product

• ZORBAX PrepHT columns are designed for rapid scale-up from the ZORBAX family of phases• Scalable prep columns are also available for Pursuit and Polaris columns• Bulk materials are available for all phases and can be ordered through Agilent’s Custom Ordering

Process, www.agilent.com/chem/customlc

Prep LC Columns

Preparative HPLC Columns

312

CoLumnS foR SmALL moLECuLE SEPARATionS

Agilent Prep columns show better resolution and loadability than competitor columns.

Superior loadability on Agilent Prep C18with basic compoundsColumn: Agilent Prep C18

443905-9024.6 x 150 mm, 5 µm

Mobile Phase: 50% 0.1%TFA:50% ACN

Flow Rate: 1 mL/min

Sample: 10 µLDoxepin/Amitriptyline0.5-50 mg/mL

LCPLC01

α = 1.6 α = 1.57

Time (min) Time (min)

mAU

mAU

0

0

500

1000

1500

2000

2500

3000

3500

4000

2 31 4 5 7 8 96 0

0

5

10

15

20

25

30

35

40

2 31 4 5 7 8 96

Agilent Prep C18 shows excellent scalability, making method transfersimple and predictable.

Column A: Agilent Prep C18443905-9024.6 x 150 mm, 5 µm

Column B: Agilent Prep C18443905-10221.2 x 150 mm, 5 µm

Column C: Agilent Prep C18413910-30230.0 x 150 mm, 10 µm

Column D: Agilent Prep C18413910-50250.0 x 150 mm, 10 µm

Mobile Phase: 55% Water:45% ACN

Flow Rate: 0.7 mL/min14.87 mL/min29.77 mL/min85.37 mL/min


Detector: 240 nm

Sample: 2 µL42.4 µL170 µL488 µL

1. Hydrocortisone2. Testosterone (in MeOH @ 1mg/mL)

A 1 2

0 2 4 6 8 1210

1

2

B

0 2 4 6 8 1210

1

2

C

0 2 4 6 8 1210

LCPLC02Time (min)

1

2

D

0 2 4 6 8 1210

Competitor W-C18Agilent Prep C18


Bonded Phase Pore SizeSurface

Area Temp. Limits pH Range Endcapped Carbon LoadC18 100Å 400 m2/g 60 °C* 2.0-10.0 Single 24%Silica 100Å 400 m2/g ** 1.0-8.0 N/A N/A

Specifications represent typical values only.*Temperature limits are 60 °C up to pH 8, 40 °C from pH 8-10.**Temperature limits for bare silica are determined by the pH of the mobile phase.

Steroids: Easy scalability using Agilent Prep columns



agilent Prep LC Columns

Hardware Description size (mm)Particle size

(µm) C18 silicastandard Columns (no special hardware required)

Scalar 4.6 x 250 10 440910-902 440910-901Scalar 4.6 x 150 10 443910-902 443910-901Scalar 4.6 x 100 10 449910-902Scalar 4.6 x 250 5 440905-902 440905-901Scalar 4.6 x 150 5 443905-902 443905-901Scalar 4.6 x 100 5 449905-902 449905-901Scalar 4.6 x 50 5 446905-902 446905-901

PrepHt Cartridge Columns (require endfittings kit 820400-901)*PrepHT 21.2 x 250 10 410910-102 410910-101PrepHT 21.2 x 150 10 413910-102 413910-101PrepHT 21.2 x 50 10 446910-102PrepHT 21.2 x 150 5 443905-102 443905-101PrepHT 21.2 x 100 5 449905-102 449905-101PrepHT 21.2 x 50 5 446905-102 446905-101PrepHT Endfittings, 2/pk 820400-901 820400-901

standard Columns (no special hardware required)Prep 30 30.0 x 250 10 410910-302 410910-301Prep 30 30.0 x 150 10 413910-302 413910-301Prep 30 30.0 x 100 10 419910-302 419910-301Prep 30 30.0 x 100 5 449905-302 449905-301Prep 30 30.0 x 50 5 446905-302 446905-301Prep 50 50.0 x 250 10 410910-502 410910-501Prep 50 50.0 x 150 10 413910-502 413910-501Prep 50 50.0 x 100 10 419910-502 419910-501Prep 50 50.0 x 100 5 449905-502 449905-501

guard Columns (hardware required)PrepHT Guard Cartridges, 2/pk 21.2 x 10 10 420212-902 420212-901Guard Cartridge Hardware 820444-901 820444-901PrepHT External Guard Hardware Kit 420420-901 420420-901Bulk Packing (1 kg) 10 420910-902 420910-901

*All PrepHT cartridge columns require hardware kit P/N 820400-901. If a guard column is desired for the 21.2 mm idcolumns, the PrepHT Guard Hardware Kit, P/N 820444-901, is also required. If the guard column is used on a 30 mm idcolumn then the external guard column hardware kit, P/N 420420-901, is required.

314


ZorBaX PrepHt• Easy scale-up from analytical to preparative scale with ZORBAX phases• Fast preparative separations, up to 2000 mg• 5 to 7 µm particles for high efficiency and high yield• Easy to install finger-tight connections seal up to 5000 psi/350 bar• Use to maintain selectivity of the analytical phase in your prep separations

High purity, high recovery and high throughput can be easily achieved with Agilent ZORBAX PrepHTcolumns. These are available in a variety of bonded phases – Eclipse XDB, StableBond, Bonus-RP, andExtend-C18 – for optimized resolution and loadability under any conditions.

ZORBAX PrepHT columns are packed with 5 and 7 µm particle sizes for very high resolution. The highresolution allows high loadability, high yield, and high purity of compounds. The larger diameter columnsand mechanically stronger ZORBAX particles allow for flow rates up to 100 mL/min, thus increasingthroughput.

ZORBAX PrepHT columns are designed for rapid scale-up from analytical to preparative scale without losingresolution. For complex separations on larger columns (21.2 mm id, 150 mm length and longer), Agilent hascarefully chosen the 7 µm particle size to achieve a balance between high efficiency and high loadability.

ZORBAX PrepHT Columns



Mass-based fraction collection using ZORBAX SB-C18 column shows high purity and high recovery of each compound (Application Note publication number 5988-7113EN).The separation of the three antianginal drugs was successfully done in a single run with high recovery and >90% purity. Separations up to 2000 mg are possible depending on the complexity of separation.

High purity and high recovery with ZorBaXPrepHt columnsSample: Antianginal drugs

amount nifedipine [mg]

amount nifmodipine [mg]

amount nifsoldipine [mg]

fraction 1 18.90 0.11 0.16 Purity Nifedipine 98.6%

fraction 2 0.29 17.66 0.77 Purity Nifmodipine 94.4%

fraction 3 0.49 1.66 18.36 Purity Nifsoldipine 89.5%

recovery [mg] 19.68 19.43 19.29recovery [%] 101.3 102.0 101.9

LCPHT01

Vial 1 – 347

Vial 2 – 343

Vial 3 – 389

21DMSO DAD

MSD

3

Time (min)2 310 4 5 76

2000000

4000000

6000000

8000000

Time (min)2 310 4 5 76

Abso

rban

ce (m

AU) 1. Nifedipine

2. Nifmodipine3. Nifsoldipine

316


ZORBAX PrepHT columns are designed for rapid scale-up from analytical to preparative scale without losing resolution. For complex separations for larger columns (21.2 mm id and higher, 150 mm length and higher), Agilent has carefully chosen the 7 µm particle size to achieve a balance between highefficiency and high loadability.

scale-up from analytical to prep ZorBaX sB-C18 columns using the same pump

Column sizeflow

(mL/min)injection

(µL) Detector Cell Part no.Column 1 50 x 150 mm 100 2200 0.3 mm quartz Custom ColumnColumn 2 21.2 x 150 mm 18 400 0.3 mm quartz 877150-102Column 3 9.4 x 150 mm 3.5 80 0.3 mm quartz 883975-202Column 4 4.6 x 150 mm 0.85 2.0 3 mm SS 883975-902Using the same 1100 pump, a scale-up from 4.6 mm to 50 mm id was possible without any loss of resolution. This increasesthroughput by reducing the time required for redeveloping and adjusting the method.

Scale-up to PrepHT

Abso

rban

ce (m

AU)

LCPHT_ScaleUp

Time (min)

1

23

Column 1

Column 2

Column 3

Column 4

0 20.05.02.5 7.5 10.0 12.5 15.0 17.5

0

1500

1000

500

2000

2500

3000

3500

1. Theobromine2. Theophylline3. Caffeine



ZorBaX PrepHt 80stableBond (require hardware 820400-901)


(µm)sB-C18usP L1

sB-C8usP L7 sB-aq

sB-CnusP L10

sB-PhenylusP L11

PrepHT Cartridge 21.2 x 250 7 877250-102 877250-106 877250-114 877250-105 877250-112PrepHT Cartridge 21.2 x 150 7 877150-102 877150-106 877150-114PrepHT Cartridge 21.2 x 150 5 870150-902 870150-906 870150-914PrepHT Cartridge 21.2 x 100 5 870100-902 870100-906 870100-914PrepHT Cartridge 21.2 x 50 5 870050-902 870050-906 870050-914PrepHT Guard Cartridge, 2/pk 17.0 x 7.5 5 820212-920 820212-915 820212-933 820212-933 820212-915

ZorBaX PrepHt 300stableBond (require hardware 820400-901)


(µm)300sB-C18usP L1

300sB-C8usP L7

300sB-C3usP L56

300sB-CnusP L10

PrepHT Cartridge 21.2 x 250 7 897250-102 897250-106 897250-109 897250-105PrepHT Cartridge 21.2 x 150 7 897150-102 897150-106 897150-109PrepHT Cartridge 21.2 x 150 5 895150-902 895150-906 895150-909PrepHT Cartridge 21.2 x 100 5 895100-902 895100-906 895100-909PrepHT Cartridge 21.2 x 50 5 895050-902 895050-906 895050-909PrepHT Guard Cartridge, 2/pk 17.0 x 7.5 5 820212-921 820212-918 820212-924 820212-924Guard Cartridge HardwareIncludes guard column end fitting, polymeric seal, and seal insertion tool (seal holder and seal pusher)

820444-901 820444-901 820444-901 820444-901

PrepHT Endfittings, 2/pk 820400-901 820400-901 820400-901 820400-901

ZorBaX PrepHt original (require hardware 820400-901)


(µm)oDs (C18)usP L1

C8usP L7

CnusP L10

nH2usP L8

siLusP L3

PrepHT Cartridge 21.2 x 250 7 877952-102 877952-106 877952-105 877952-108 877952-101PrepHT Endfittings, 2/pk 820400-901 820400-901 820400-901 820400-901 820400-901

318


ZorBaX PrepHt eclipse XDB (require hardware 820400-901)

Hardware Description size (mm) Particle size (µm)

eclipseXDB-C18usP L1

eclipseXDB-C8usP L7

PrepHT Cartridge 21.2 x 250 7 977250-102 977250-106PrepHT Cartridge 21.2 x 150 7 977150-102 977150-106PrepHT Cartridge 21.2 x 150 5 970150-902 970150-906PrepHT Cartridge 21.2 x 100 5 970100-902 970100-906PrepHT Cartridge 21.2 x 50 5 970050-902 970050-906PrepHT Guard Cartridge, 2/pk 17.0 x 7.5 5 820212-925 820212-926Guard Cartridge HardwareIncludes guard column end fitting, polymeric seal, and seal insertion tool (seal holder and seal pusher)

820444-901 820444-901

PrepHT Endfittings, 2/pk 820400-901 820400-901

ZorBaX PrepHt Bonus-rP and extend-C18 (require hardware 820400-901)

Hardware Description size (mm) Particle size (µm)Bonus-rPusP L60

extend-C18usP L1

PrepHT Cartridge 21.2 x 250 7 878250-101PrepHT Cartridge 21.2 x 150 7 878150-101PrepHT Cartridge 21.2 x 150 5 868150-901 770150-902PrepHT Cartridge 21.2 x 100 5 868100-901 770100-902PrepHT Cartridge 21.2 x 50 5 868050-901 770050-902PrepHT Guard Cartridge, 2/pk 17.0 x 7.5 5 820212-928 820212-930Guard Cartridge HardwareIncludes guard column end fitting, polymeric seal, and seal insertion tool (seal holder and seal pusher)

820444-901 820444-901


ZorBaX PrepHt rx-siL (require hardware 820400-901)

Hardware Description size (mm) Particle size (µm)rx-siLusP L3

rx-C18usP L1

PrepHT Cartridge 21.2 x 250 7 877250-101PrepHT Cartridge 21.2 x 250 7 877967-102PrepHT Guard Cartridge, 2/pk 17.0 x 7.5 5 820212-919 820212-914Guard Cartridge HardwareIncludes guard column end fitting, polymeric seal, and seal insertion tool (seal holder and seal pusher)

820444-901 820444-901


ZorBaX PrepHt accessoriesHardware Description Part no.

Guard Cartridge Hardware 820444-901PrepHT Endfittings, 2/pk 820400-901Replacement Seals 820385-901



230220210200190180170160150140130120110100

908070605040302010

0

109.598.587.576.565.554.543.532.521.510.50

109.598.587.576.565.554.543.532.521.510.50

109.598.587.576.565.554.543.532.521.510.50

1

2

RT [min]

RT [min]

RT [min]

mAU

200190180170160150140130120110100

908070605040302010

0-10

mAU

240

220

200

180

160

140

120

100

80

60

40

20

0

mAU

• Prep-scalable columns for Pursuit and Pursuit XRs columns• Particle sizes to 10 µm and column diameters up to 50 mm• High surface area silica

Pursuit and Pursuit XRs Prep columns are designed for high loadability with a high surface area.

natural products – capsaicin and dihydrocapsaicinon Pursuit Xrs C18Column a: Pursuit Xrs C18

a6001150X0464.6 x 150 mm, 3 µm

Column B: Pursuit Xrs C18a6000150X0464.6 x 150 mm, 5 µm

Column C: Pursuit Xrs C18a3002150X0464.6 x 150 mm, 10 µm

Mobile Phase: CH3CH:H20 - 70:30



Detector: 220 nm

Sample: 1. Capsaicin2. Dihydrocapsaicin

Demonstrating an easy, linear scale-up of natural products fromPursuit XRs C18 3 µm and 5 µm analytical columns to a 10 µmpreparative column.

Pursuit and Pursuit Xrs Prep

10 µm

5 µm

3 µm

320


agilent Pursuit Prep Columns

size (mm)Particle size

(µm)Pursuit C18usP L1

Pursuit C8usP L7 Pursuit Diphenyl Pursuit PfP

10.0 x 250 5 A3000250X100 A3030250X100 A3040250X100 A3050250X10010.0 x 250 10 A6002250X100 A3032250X10021.2 x 250 10 A6002250X21221.2 x 250 10 A6002250X212 A3032250X212

agilent Pursuit Xrs Prep Columns


(µm)

PursuitXrs C18usP L1

Pursuit Xrs C8usP L7

PursuitXrs Diphenyl

PursuitXrs siusP L3

21.2 x 250 10 A6002250X212 A6004250X21221.2 x 250 5 A6000250X212 A6020250X21221.2 x 150 5 A6000150X212 A6010150X21221.2 x 100 5 A6000100X212 A6010100X212 A6020100X21221.2 x 50 5 A6000050X21230.0 x 250 10 A6002250X300 A6004250X30030.0 x 150 10 A6002150X30030.0 x 250 5 A6000250X300 A6010250X30030.0 x 150 5 A6000150X30030.0 x 100 5 A6000100X30050.0 x 250 10 A6002250X500 A6022250X500 A6004250X500



• Prep-scalable columns for Polaris phases• 10.0 and 21.2 mm ids available, with particles up to 10 µm

scale-up from analytical to prepColumn a: Polaris C18-a

a2001050X0464.6 x 50 mm, 3 µm

Column B: Polaris C18-aa2000050X0464.6 x 50 mm, 5 µm

Column C: Custom columnMobile Phase: A: H20 + 0.1% NH40H, pH 10.0 (25 mM)

B: CH3CNA:B 65:35


Temperature: 40 °C

Detector: 215 nm

Sample: 1. Pindolol2. Metoprolol3. Propranolol

Polaris Prep Columns


(µm)PolarisC18-a

PolarisC18-ether

Polarisamide C18

Polarissi-a

PolarisC8-a

PolarisC8-ether

PolarisnH2

10.0 x 250 5 A2000250X100 A2020250X100 A2006250X100 A2010250X100 A2030250X100 A2013250X10021.2 x 250 5 A2000250X212 A2030250X212 A2003250X212 A2010250X212 A2013250X21221.2 x 250 10 A2002250X212 A2004250X212

Polaris Prep Columns

C: 10 µm

B: 5 µm

a: 3 µm

Bulk materials for prepAgilent has bulk materials available for all phases. Most materials and quantities can be ordered through the Custom Column and Bulk Ordering process,and can be produced in multiple kg. quantities. Quotes are able to be delivered within 48 hours. Contact your Agilent product specialist for support in placinga custom order.

1

23

1

23

1

23

322


Agilent offers a complete range of Load & Lock column systems for laboratory and process preparative LC. They are designed to let you easily and quickly pack your own preparative high efficiency columns. This is the right solution for applications ranging in scale from development (multigrams) to production(multi-kilo) of pharmaceutical compounds, peptides, and natural products. Our Load & Lock columns have a unique fluid/sample distribution system to maximize productivity. The system provides dynamic axial compression (DAC) and static "locked" axial compression (SAC) and is designed for easy operation to deliver greater convenience.

Laboratory Load & Lock Columns• Mobile packing station supports three different column sizes• Runs on compressed air with no need for a power supply• Quick and easy packing and unpacking within minutes

Agilent's laboratory scale Load & Lock columns combine excellent packed-bed stability with enhanced flowdistribution to deliver the highest quality purification possible with maximum speed, flexibility, and ease ofoperation. Three different column sizes are supported: 1 in, 2 in and 3 in id. Because the station is poweredby compressed air, it is the perfect solution for hazardous environments. The quick-release single bolt clampoffers speedy and easy packing and unpacking within minutes.

Load & Lock Preparative HPLC Column Packing systemsDescription water Jacket size (mm) Part no.Load & Lock 4001 Column No 25.0 x 500 PCG93LL500X25

Yes 25.0 x 500 PCG93LL500X25WJSpare parts kit PCG931AAKIT

Load & Lock 4002 Column No 50.0 x 500 PCG93LL500X50Yes 50.0 x 500 PCG93LL500X50WJSpare parts kit PCG932AAKIT

Load & Lock 4003 Column No 75.0 x 500 PCG93LL500X75Yes 75.0 x 500 PCG93LL500X75WJSpare parts kit PCG933AAKIT

Mobile packing station (air driven hydraulic) PCG93LLSTAND123

Load & Lock Preparative HPLC ColumnPacking systems

Load & Lock Columns



Columns for Other HPLC Techniques

Reproducible results for Normal Phase and beyondAgilent's extended family of HPLC columns support every technique, providing you with the Agilent quality you depend on for every application.

• ZORBAX HILIC Plus – good retention of small, polar analytes and high sensitivity for LC/MS – in Fast LC 1.8 µm options

• ZORBAX normal phase columns – bonded and non-bonded silica packings • ZORBAX ion-exchange columns – based on rugged ZORBAX Silica, stable from pH 2-7• Hi-Plex columns for carbohydrate analysis – ligand-exchange columns• Ultron ES Chiral columns – with two complimentary protein-based chiral stationary phases –

are an excellent choice for enantiomeric separations. Ideal for many pharmacological applications.

324


• HILIC column for good retention of small, polar analytes• Based on Eclipse Plus silica for excellent peak shape• High sensitivity for LC/MS applications • Recommended for EPA Method 1694

Agilent ZORBAX HILIC Plus columns are for use in hydrophilic interaction chromatography (HILIC)applications, which are typically used for the retention and resolution of small polar compounds. HILIC Pluscolumns are non-bonded silica columns based on the high performance silica used in ZORBAX Eclipse Pluscolumns. This silica provides excellent peak shape, critical for many polar, basic analytes. These columnsship prepared for use in HILIC mode – containing acetonitrile:water – in order to reduce the extensiveequilibration typically required for HILIC separations. HILIC Plus columns are available in a 3.5 µm particlesize for high resolution and in 2.1 and 4.6 mm id for compatibility with mass spectrometers or with standardUV detectors.

Column specifications

Phase Pore size surface area pH rangeNon-bonded silica 95Å 160 m2/g 0-8.0


ZorBaX HiLiC Plus

tiPs & tooLs

Poroshell 120 HILIC is very similar to ZORBAX HILIC Plus.

Turn to page 228



separation of group 4 analytes in ePa 1694on ZorBaX HiLiC Plus columnColumn: ZorBaX HiLiC Plus

959793-9012.1 x 100 mm, 3.5 µm

Mobile Phase: 90% Acetontrile:10% Water


Gradient: Linear gradient to 55% acetonitrile in 7 minHeld at 55%

Temperature: 25 °C

Duplicate runs for column USCJP0004; 10 min equilibration between two runs

EPA1694 0.5 1.0 1.5 2.0 2.5 3.0 3.5 4.0 4.5 5.0 5.5 6.0 6.5 7.0 7.5 8.0 8.5 9.0 9.5 10.0 10.5 11.0 11.5 12.0 12.5 13.0 13.5 14.0 14.5 15.0 15.5 16.0 16.5 17.0 17.5 18.0 18.5 19.0 19.5 20.0 20.5 21.0 21.5 22.0 22.5 23.0 23.5 24.0 24.5

0.950.900.850.800.750.700.650.600.550.500.450.400.350.300.250.200.150.100.05

0

1.00x102

0.950.900.850.800.750.700.650.600.550.500.450.400.350.300.250.200.150.100.05

0

1.00x102

ZorBaX HiLiC PlusDescription size (mm) Particle size (µm) Part no.Analytical 4.6 x 100 3.5 959961-901Analytical 4.6 x 50 3.5 959943-901Narrow Bore 2.1 x 100 3.5 959793-901Narrow Bore 2.1 x 50 3.5 959743-901

Cimetidine

albuterol

ranitidine

metformin

ZorBaX HiLiC Plus rrHD, stable to 1200 barsize (mm) Particle size (µm) Part no.3.0 x 100 1.8 959758-3013.0 x 50 1.8 959757-3012.1 x 150 1.8 959759-9012.1 x 100 1.8 959758-9012.1 x 50 1.8 959757-901

Poroshell 120 HiLiC Plussize (mm) Particle size (µm) Part no.2.1 x 50 2.7 699775-9012.1 x 100 2.7 695775-9012.1 x 150 2.7 693775-9013 x 50 2.7 699975-3013 x 150 2.7 693975-3014.6 x 50 2.7 699975-9014.6 x 100 2.7 695975-9014.6 x 150 2.7 693975-901

326


For normal-phase chromatography, the Agilent ZORBAX product line offers a choice of bonded and non-bonded silica packings.

ZORBAX Rx-SIL

ZORBAX Eclipse XDB-CN• Made from highly pure Rx-SIL• Excellent choice for normal-phase applications with basic compounds• Equilibrates more rapidly than ZORBAX Rx-SIL and is used for many of the same

normal-phase applications

ZorBaX normal-Phase Columns

• Made from highly pure (> 99.995%) porous silica microspheres (pore size is the space between thesolid silica microparticles)

• Available in 1.8 and 5 µm particle sizes• Stronger than other silica types• Less acidic than ZORBAX SIL, lower metal content• Low acidity and low metal content make ZORBAX Rx-SIL ideal for normal-phase separation of polar

compounds that exhibit poor peak symmetry on more acidic silica• Useful for very hydrophilic compounds with high organic mobile phases in HILIC mode



ZORBAX CN• Cyanopropyldimethylsilane monolayer bonded to ZORBAX SIL• Equilibrates more rapidly than ZORBAX SIL, and used for many of the same normal-phase applications• Less prone to fouling and less water sensitive than silica

Polaris NH2• 180Å silica for high surface area and loadability• 5.5% carbon load• Available in 3 µm, 5 µm, and 10 µm sizes• Polar-modified with silanol shielding• Designed for high-aqueous conditions

Pursuit XRs Si• 100Å silica for higher surface area and good loadability• 14.6% carbon load• Available in 3 µm, 5 µm and 10 µm

High resolution normal-phase separation ofoctylphenoxy ethanol surfactant on ZorBaX CnColumn: ZorBaX Cn

880952-7054.6 x 250 mm, 5 µm

Mobile Phase: Primary: HeptaneSecondary: 2-Methoxyethanol/Isopropanol (50/50)

Flow Rate: 2 mL/min

Gradient: 2-20% Secondary in 10 min, Linear Hold at 20%

Temperature: 50 °C

Detector: 278 nm

Sample: Octylphenoxy (polyethylene oxy)Ethanol Surfactant (n=10)

LCNP001Time (min)

2010 150 5

Polaris Si-A

291-297Pursuit ordering information can be found on pages

300-303Polaris ordering information can be found on pages

• 180Å silica with highest surface area and loadability• Available in 3 µm, 5 µm, and 10 µm

328



Phase Pore size surface area pH range endcapped Carbon LoadZORBAX Rx-SIL 80Å 180 m2/g 0-8.0 NoZORBAX Eclipse XDB-CN 80Å 180 m2/g 2.0-8.0 Yes 4.3%ZORBAX SIL 70Å 300 m2/g 0-8.0 NoZORBAX CN 70Å 300 m2/g 2.0-7.0 Yes 7%ZORBAX NH2 70Å 300 m2/g 2.0-7.0 Yes 4%

Pursuit XRs Silica is anotherchoice for normal-phasechromatography. For moreinformation, see pages

ZORBAX NH2• Amino-propyl silane phase bonded to ZORBAX SIL• Used for normal-phase and weak anion-exchange, and reversed-phase HPLC of polar compounds• Vitamins A and D are separated in the normal-phase mode• Carbohydrates and sugars are separated in the reversed-phase mode

tiPs & tooLs

295-296.



normal-Phase Columns Based on ZorBaX rx-siL

Hardware Description size (mm) Particle size (µm)rx-siL**usP L3

eclipseXDB-CnusP L10

standard Columns (no special hardware required)Semi-Prep 9.4 x 250 5 880975-201Analytical 4.6 x 250 5 880975-901 990967-905*Analytical 4.6 x 150 5 883975-901 993967-905*Rapid Resolution HT, 600 bar 4.6 x 100 1.8 828975-901Rapid Resolution HT, 600 bar 4.6 x 50 1.8 827975-902Rapid Resolution HT, 600 bar 3.0 x 100 1.8 828975-301Rapid Resolution HT, 600 bar 3.0 x 50 1.8 827975-301Narrow Bore 2.1 x 150 5 883700-901 993700-905*Rapid Resolution HT, 600 bar 2.1 x 100 1.8 828700-901Rapid Resolution HT, 600 bar 2.1 x 50 1.8 827700-901

guard Columns (hardware required)Guard Cartridge, 2/pk 9.4 x 15 5 820675-119Guard Cartridge, 4/pk 4.6 x 12.5 5 820950-919 820950-935Guard Cartridge, 4/pk 2.1 x 12.5 5 821125-919 821125-935Guard Hardware Kit 9.4 x 15 840140-901Guard Hardware Kit 820999-901 820999-901

PrepHt Cartridge Columns (require endfittings kit 820400-901)PrepHT Cartridge 21.2 x 250 7 877250-101PrepHT Endfittings, 2/pk 820400-901PrepHT Guard Cartridge, 2/pk 17.0 x 7.5 5 820212-919Guard Cartridge Hardware 820444-901

*These columns ship containing reversed-phase solvents. Flush with isopropanol before using normal-phase solvents.**These columns can also be used in HILIC mode.

330


normal-Phase Columns Based on ZorBaX original siL


(µm)siLusP L3

CnusP L10

nH2usP L8

Carbohydrateanalysis*

standard Columns (no special hardware required)Semi-Prep 9.4 x 250 5 880952-201 880952-205 880952-208Analytical 4.6 x 250 5 880952-701 880952-705 880952-708 840300-908Analytical 4.6 x 150 5 883952-701 883952-705 883952-708 843300-908Narrow Bore 2.1 x 50 5 860700-708

guard Columns (hardware required)Guard Cartridge, 2/pk 9.4 x 15 5 820675-119 820675-111 820675-111Guard Cartridge, 4/pk 4.6 x 12.5 5 820950-901 820950-905 820950-908 820950-908Guard Cartridge, 4/pk 2.1 x 12.5 5Guard Hardware Kit 9.4 x 15 840140-901 840140-901 840140-901Guard Hardware Kit 820999-901 820999-901 820999-901 820999-901

PrepHt Cartridge Columns (require endfittings kit 820400-901)PrepHT Cartridge 21.2 x 250 7 877952-101 877952-105 877952-108PrepHT Endfittings, 2/pk 820400-901 820400-901 820400-901Guard Cartridge Hardware 820444-901

*Columns ship in acetonitrile:water and are tested with a mix of sugars.



Pursuit Xrs si, usP L3size (mm) Particle size (µm) Part no.semi-Prep scale10.0 x 250 10 A6004250X100analytical scale4.6 x 250 10 A6004250X0464.6 x 100 5 A6006100X0464.6 x 50 5 A6006050X0464.6 x 100 3 A6005100X0464.6 x 50 3 A6005050X0462.1 x 100 5 A6006100X0212.0 x 50 3 A6005050X020Prep scale50.0 x 250 10 A6004250X50030.0 x 250 10 A6004250X30021.2 x 250 10 A6004250X212


size (mm) Particle size (µm)PolarisnH2

Polarissi-a

50.0 x 250 10 A2004250X50021.2 x 250 10 A2004250X21221.2 x 250 5 A2013250X212 A2003250X21221.2 x 150 5 A2003150X04621.2 x 50 5 A2003050X21210.0 x 250 5 A2013250X100

(Continued)

332


metaguard ColumnsHardware Dimensions Particle size (µm) Polaris nH2 Polaris si-a

4.6 10 A2004MG2.0 10 A2004MG24.6 5 A2013MG A2003MG2.0 5 A2013MG2 A2003MG24.6 3 A2014MG A2005MG2.0 3 A2014MG2 A2005MG2

4.6 x 250 10 A2003250X0464.6 x 250 5 A2013250X0464.6 x 150 5 A2013150X046 A2003150X0464.6 x 100 5 A2013100X046 A2003100X0464.6 x 50 5 A2013050X046 A2003050X0464.6 x 250 3 A2014250X046 A2005250X0464.6 x 150 3 A2014150X046 A2005150X0464.6 x 100 3 A2014100X046 A2005100X0464.6 x 50 3 A2014050X046 A2005050X0464.0 x 250 5 A2013250X040 A2003250X0404.0 x 150 5 A2013150X040 A2003150X0404.0 x 125 5 A2013125X040 A2003125X0403.0 x 250 5 A2013250X030 A2005250X0463.0 x 150 5 A2013150X030 A2003150X0303.0 x 100 5 A2013100X030 A2003100X0303.0 x 50 5 A2003050X0303.0 x 250 3 A2014250X030 A2003250X0303.0 x 150 3 A2014150X030 A2005150X0303.0 x 100 3 A2014100X030 A2005100X0303.0 x 50 3 A2014050X030 A2005050X0302.0 x 250 5 A2013250X020 A2003250X0202.0 x 150 5 A2013150X020 A2003150X0202.0 x 100 5 A2013100X020 A2003100X0202.0 x 50 5 A2013050X020 A2003050X0202.0 x 30 5 A2013030X020 A2003030X0202.0 x 20 5 A2013020X020 A2003020X0202.0 x 250 3 A2014250X020 A2005250X0202.0 x 150 3 A2014150X020 A2005150X0202.0 x 100 3 A2014100X020 A2005100X0202.0 x 50 3 A2014050X020 A2005050X0202.0 x 30 3 A2014030X020 A2005030X0202.0 x 20 3 A2014020X020 A2005020X020

size (mm) Particle size (µm)PolarisnH2

Polarissi-a




• ZORBAX SAX and 300SCX columns are based on rugged ZORBAX silica• Stable from pH 2-7• Provide high efficiency, rapid separations• Compatible with organic mobile phase modifiers

Agilent ZORBAX Strong Ion-Exchange columns are available as both Strong Anion-Exchange (SAX) andStrong Cation-Exchange (300SCX) columns. Each column is packed with bonded, 5 µm, spherical silicaparticles for optimum efficiency.

ZORBAX SAX packing has a permanently bonded quaternary amine. A trifunctional organo-silane reagent isused in producing this packing to maximize its stability with aqueous mobile phases. This column is ideal forseparation of water-soluble compounds such as aromatic and aliphatic carboxylic acids and sulfonic acids.

ZORBAX SCX packing has 300Å pore size silica particles chemically bonded to an aromatic sulfonic acidgroup. This column is used for separations of basic, water-soluble compounds and bio-molecules.


Bonded Phase Pore size surface area pH range functionality max PressureZORBAX SAX 70Å 300 m2/g 2.0-7.0 Quaternary amine 350 barZORBAX 300SCX 300Å 50 m2/g 2.0-7.0 Sulfonic acid 350 bar


ZorBaX ion-exchange Columns – saX and sCX

Ion-Exchange Columns

334


Cough/cold remedies on ZorBaX 300sCXColumn: ZorBaX 300sCX

880952-7044.6 x 250 mm, 5 µm

Mobile Phase: 100 mM NaH2PO4 (pH 6.5)

Flow Rate: 3 mL/min

Temperature: 20 °C

Detector: 210 nm

Sample: Cold remedies

1. Pyrilamine2. Theophylline3. Glyceryl Guaicolate4. Caffeine5. Phenylephrine

LCIE001Time (min)0 2 4

1

23 4 5

ZorBaX ion-exchange Columns – saX and sCX

Description size (mm)Particle size

(µm) saX 300sCXSemi-preparative 9.4 x 250 5 880952-203 880952-204Analytical 4.6 x 250 5 880952-703 880952-704Analytical 4.6 x 250 5 880952-714*Analytical 4.6 x 150 5 883952-703 883952-704Analytical 4.6 x 150 5 883952-714*Analytical 4.6 x 50 5 846952-704Solvent Saver 3.0 x 50 5 860700-304Narrow Bore 2.1 x 150 5 883700-704Narrow Bore 2.1 x 150 5 883700-714*Narrow Bore 2.1 x 50 5 860700-704Guard Hardware Kit 820999-901 820999-901*These columns have been modified to provide less retention, for those who desire that in their application.



Hi-Plex columns are engineered with monodisperse sulfonated particles, creating a high-performancemedia uniquely suited to stringent USP methods for analyzing carbohydrates, alcohols and organic acids.Unlike the ZORBAX NH2 column used for carbohydrate analysis with an acetonitrile:water mobile phase, Hi-Plex ligand-exchange columns provide more resolution for mono- and disaccharides due to theinteraction of the hydroxyl groups with the metal ion associated with the cation-exchange functionalityof the sulfonic acid group.


Bonded Phasetemperature

rangeflow rate(mL/min) eluent

Hi-Plex Ca 80-90 °C 0.6 WaterHi-Plex Ca USP L19 80-90 °C 0.3 WaterHi-Plex Pb 70-90 °C 0.6 WaterHi-Plex H for carbohydrates 60-70 °C 0.6 WaterHi-Plex H for organic acids 40-60 °C 0.6 Dilute AcidHi-Plex Ca (Duo) 80-90 °C 0.6 WaterHi-Plex K 80-90 °C 0.6 WaterHi-Plex Na (Octo) 80-90 °C 0.6 Water, Sodium HydroxideHi-Plex Na 80-90 °C 0.3 Water

Hi-Plex Columns for Carbohydrate analysis• Agilent's recommended column for accurate, low-pressure analysis of typical carbohydrates,

providing leading-edge features for reliable quantitative and qualitative analysis• Enable reduced column operating pressures for repeatable performance and longer column life• Wide range of ligand counter ions and column configurations meet requirements of challenging

organic applications• Simplified HPLC system requirements through isocratic separation capabilities; excellent

batch-to-batch reproducibility for ultimate confidence in your results• Can be used with water or diluted acid as an eluent• Available in 8 µm and 10 µm particle sizes in a range of choices for USP media types – L17,

L19, L34 and L58

The least complicated LC methods for detecting sugars, sugar alcohols and organic acids call for ligand-exhange columns with a simple mobile phase. However, the wide particle size distribution of conventional resins can lead to high backpressures and reduced productivity.

336


USP methods specify the type of HPLC media and column dimensions which should be used for the analysis. The Hi-Plex product range has four materials that comply with USP definitions.

Strong cation-exchange resin consisting of sulfonated, cross-linked styrene-divinylbenzene copolymer in the hydrogen form, 7 to 11 µm in diameter – Hi-Plex H.

Strong cation-exchange resin consisting of sulfonated, cross-linked styrene-divinylbenzene copolymer in the calcium form, 9 µm in diameter – Hi-Plex Ca and Hi-Plex Ca (Duo).

Strong cation-exchange resin consisting of sulfonated, cross-linked styrene-divinylbenzene copolymer in the lead form, about 9 µm in diameter – Hi-Plex Pb.

Strong cation-exchange resin consisting of sulfonated, cross-linked styrene-divinylbenzene copolymer in the sodium form, 6 to 30 µm diameter – Hi-Plex Na and Hi-Plex Na (Octo).

In addition to the standard column sizes, the media is also packed in specific column dimensions for different USP methods, including sugar alcohol analysis.

For some application areas there are several column options, and the choice of the most appropriate Hi-Plex media will depend on sample matrix and exact carbohydrate composition.

media type L58

media type L34

media type L19

media type L17

Hi-Plex Column Selection



Hi-Plex Column selection

application area recommended ColumnUSP Methods Specifying L17 Media Hi-Plex HUSP Methods Specifying L19 Media Hi-Plex Ca and Hi-Plex Ca (Duo)USP Methods Specifying L34 Media Hi-Plex PbUSP Methods Specifying L58 Media Hi-Plex Na and Hi-Plex Na (Octo)Mono- and Disaccharides Hi-Plex Ca

Hi-Plex PbHi-Plex HHi-Plex Na (Octo)

Anomer Separations Hi-Plex CaOrganic Acids Hi-Plex HAlcohols Hi-Plex Ca

Hi-Plex KHi-Plex HHi-Plex Pb

Adulteration of Food and Beverages Hi-Plex Ca and Hi-Plex PbFood Additives Hi-Plex Ca and Hi-Plex PbDairy Products Hi-Plex Ca and Hi-Plex HSweetened Dairy Products Hi-Plex PbConfectionery Hi-Plex Ca and Hi-Plex PbFruit Juice Hi-Plex CaWine Hi-Plex HWood Pulp Hydrolysates (cellulose/hemi-cellulose) Hi-Plex PbFermentation Monitoring Hi-Plex HOligosaccharides Hi-Plex NaSamples with High Salt Content (molasses) Hi-Plex Na (Octo)Oligosaccharides <Dp5 with Monosaccharides Hi-Plex Ca (Duo)Corn Syrups Hi-Plex Na

338


1. Sucrose2. Glucose3. Fructose4. Sorbitol

analysis of fruit juiceColumn: Hi-Plex Ca

PL1170-68107.7 x 300 mm, 8 µm

Mobile Phase: Water


Temperature: 85 °C

Detector: RI

1 2

3

4

1

2 3

1

2 3

VLC0009

0 min 25

0 min 20

0 min 20

1. Oxalic acid2. Citric acid3. Tartaric acid4. Succinic acid5. Lactic acid

organic acid analysisColumn: Hi-Plex H

PL1170-68307.7 x 300 mm, 8 µm

Mobile Phase: Water with acid as specified


Temperature: 60 °C

Detector: ELS (neb=80 °C, evap=90 °C, gas=0.7 SLM), RI

12 3

4 5

12 3

4 5

VLC0010

0 min 15

0 min 15

orange juice

tomato juice

apple juice

0.1% tfa using eLs

5 mm H2so4 using ri

12

3 45 6

7

VLC00110 min 25



1. Iso-erythritol2. Adonitol3. Arabitol4. Mannitol5. Xylitol6. Dulcitol7. Sorbitol

usP methods for sugar alcoholsColumn: Hi-Plex Ca usP L19

PL1570-58104.0 x 250 mm, 8 µm

Mobile Phase: Water


Temperature: 60 °C

Detector: RI

1. Dp12. Dp23. Dp34. Dp45. Dp56. Dp67. Dp78. Dp89. Dp9

10. Dp1011. Dp1112. Dp1213. Dp1314. Dp14

Corn syrup, Hi-PlexColumn: Hi-Plex na

PL1171-61407.7 x 300 mm, 10 µm

Mobile Phase: Water

Pressure: 11 bar


Temperature: 80 °C

Detector: RI

14-10

12

3

4

9-5

VLC0012

0 min 30

340


1 2

3

45

6

78

230 min

analysis of sweeteners on Hi-Plex Ca columnsColumn: Hi-Plex Ca

PL1170-68107.7 x 300 mm, 8 µm

Mobile Phase: Water


Temperature: 85 °C

Detector: ELSD

1. Stachyose2. Raffinose3. Sucrose4. Glucose5. Galactose6. Fructose7. Mannitol8. Sorbitol

Hi-Plex Ca columns are ideal for analyzing most sweeteners, including glucose and fructose (monosaccharides), sucrose (disaccharide), and mannitol and sorbitol (sugar alcohols).

12

3

4

150 min

analysis of carbohydates on Hi-Plex H columnsColumn: Hi-Plex H

PL1170-68307.7 x 300 mm, 8 µm

Mobile Phase: Water


Temperature: 70 °C

Detector: RI

1. Maltotriose2. Lactose3. Glucose4. Fructose

For carbohydrate analysis of samples containing high levels of organic acids, Hi-Plex H columns deliver sharp, reproducible peaks. Note, however, that some sugars (such as raffinose) can undergo acidhydrolysis even when water is used as the eluent.



32

1

230 min

analysis of sugars with high sodium matrixColumn: Hi-Plex na (octo)

PL1170-68407.7 x 300 mm, 8 µm

Mobile Phase: 0.015 M NaOH


Temperature: 85 °C

Detector: RI

1. Sucrose2. Glucose3. Arabinose

Food products containing high levels of sodium ions are best analyzed with Hi-Plex Na (Octo) columns. This saves time when sodium hydroxide is used as the eluent with PAD, because it eliminates the need for the post-column addition of sodium hydroxide.

2

1

0 min 23

usP method for sorbitolColumn: Hi-Plex Pb usP L34

PL1170-28207.7 x 100 mm, 8 µm

Mobile Phase: Water


Temperature: 50 °C

Detector: RI

1. Mannitol2. Sorbitol

USP method for sorbitol – a sugar alcohol andalternative sweetener – using mannitol as the internalstandard. Hi-Plex Pb columns are recommended foralcoholic drinks that also contain glycerol, as well assweetened dairy-based food products.

342


Hi-Plex Columns for Carbohydrate analysis

Description size (mm)Particle

size (µm)Crosslink

Content (%)Counter

ion Part no.Hi-Plex Ca USP L19 4.0 x 250 8 8 Ca2+ PL1570-5810Hi-Plex Ca (Duo) 6.5 x 300 8 8 Ca2+ PL1F70-6850Hi-Plex Ca 7.7 x 300 8 8 Ca2+ PL1170-6810Hi-Plex Pb USP L34 7.7 x 100 8 8 Pb2+ PL1170-2820Hi-Plex Pb 7.7 x 300 8 8 Pb2+ PL1170-6820Hi-Plex K 7.7 x 300 8 8 K+ PL1170-6860Hi-Plex H 6.5 x 300 8 8 H+ PL1F70-6830Hi-Plex H 7.7 x 300 8 8 H+ PL1170-6830Hi-Plex H USP L17 7.7 x 100 8 8 H+ PL1170-2823Hi-Plex Na 7.7 x 300 10 4 Na+ PL1171-6140Hi-Plex Na (Octo) 7.7 x 300 8 8 Na+ PL1170-6840

Hi-Plex guard Columns


size (µm)Crosslink

Content (%)Counter

ion Part no.Hi-Plex Ca 7.7 x 50 8 8 Ca2+ PL1170-1810Hi-Plex Ca (Duo) 7.7 x 50 8 8 Ca2+ PL1170-1850Hi-Plex Pb 7.7 x 50 8 8 Pb2+ PL1170-1820Hi-Plex K 7.7 x 50 8 8 K+ PL1170-1860Hi-Plex H 7.7 x 50 8 8 H+ PL1170-1830Hi-Plex Na 7.7 x 50 10 4 Na+ PL1171-1140Hi-Plex Na (Octo) 7.5 x 50 8 8 Na+ PL1170-1840

Hi-Plex guard Cartridges, 2/pk


size (µm)Crosslink

Content (%)Counter

ion Part no.Hi-Plex Ca 3.0 x 5.0 8 8 Ca2+ PL1670-0810Hi-Plex Ca (Duo) 3.0 x 5.0 8 8 Ca2+ PL1670-0850Hi-Plex Pb 3.0 x 5.0 8 8 Pb2+ PL1670-0820Hi-Plex K 3.0 x 5.0 8 8 K+ PL1670-0860Hi-Plex H 3.0 x 5.0 8 8 H+ PL1670-0830Hi-Plex Na 3.0 x 5.0 10 4 Na+ PL1671-0140Hi-Plex Na (Octo) 3.0 x 5.0 8 8 Na+ PL1670-0840Guard Cartridge holder for 3.0 x 5.0 mm cartridges PL1310-0016


Quick Guide to USP Designations for HPLC Columns

(Continued)

The US Pharmacopeia (USP) is a standard source for many pharmaceutical methods. The USP specifiescolumns by packing materials rather than by manufacturer. The USP has updated its L1 definitions, listedbelow you will see the most recent definitions and columns that apply. Rapid Resolution High Throughput(RRHT) columns are now choices in the L1, L7, and L11 categories.


usP Designations

usPmethod usP Packing materials Column

Particle size(µm)

Pore size(Å)

L1 Octadecyl silane chemically bonded to porous silica or ceramicmicroparticles, 1.5 to 10 µm in diameter, or a monolithic rod

Poroshell 120 EC-C18Poroshell 120 SB-C18Poroshell 300SB-C18Poroshell 300 Extend-C18ZORBAX Eclipse Plus C18ZORBAX Eclipse XDB-C18ZORBAX StableBond SB-C18ZORBAX Rx-C18ZORBAX Extend-C18ZORBAX ODSZORBAX ODS classicPursuit XRs C18Pursuit C18Pursuit C18-APolaris C18-EtherSepTech ST60 C18SepTech ST150 C18Agilent Prep C18

2.72.7551.8, 3.5, 51.8, 3.5, 5, 71.8, 3.5, 5, 73.5, 51.8, 3.5, 5, 73, 5, 753, 5, 103, 5, 103, 5, 103, 510105, 10

120120300300958080, 3008080, 300707010020018020060150100

L3 Porous silica particles, 1.5 to 10 µm in diameter, or a monolithic silicarod

ZORBAX HILIC PlusZORBAX SILZORBAX Rx-SILPursuit XRs SiPolaris Si-AAgilent Prep

1.8, 3.553.5, 5, 73, 5, 105, 105, 10

957080, 300100180100

L7 Octylsilane chemically bonded to totally porous silica particles, 1.5 to 10µm in diameter, or a monolithic silica rod

Poroshell 120 EC-C8Poroshell 120 SB-C8Poroshell 300SB-C8ZORBAX Eclipse Plus C8ZORBAX Eclipse XDB-C8ZORBAX SB-C8ZORBAX Rx-C8ZORBAX C8Pursuit XRs C8Pursuit C8Polaris C8-APolaris C8-Ether

2.72.751.8, 3.5, 51.8, 3.5, 5, 71.8, 3.5, 5, 71.8, 3.5, 5, 753, 5, 103, 5, 103, 53, 5

120120300958080, 3008070100200180200

344


(Continued)

usP Designations


Particle size(µm)

Pore size(Å)

L17 Strong cation-exchange resin consisting of sulfonated cross-linkedstyrene-divinylbenzene copolymer in the hydrogen form, 7 to 11 µm in diameter

Hi-Plex H 8 N/A

L19 Strong cation-exchange resin consisting of sulfonated cross-linkedstyrene-divinylbenzene copolymer in the calcium form, 9 µm in diameter

Hi-Plex CaHi-Plex Ca (Duo)

88

N/AN/A

L20 Dihydroxypropane groups chemically bonded to porous silica particles, 3 to 10 µm in diameter

LiChrospher Diol 5 N/A

L8 An essentially monomolecular layer of aminopropylsilane chemicallybonded to totally porous silica gel support, 3 to 10 µm in diameter

ZORBAX NH2Polaris NH2

55

70180

L9 Irregular or spherical, totally porous silica gel having a chemically bonded, strongly acidic cation-exchange coating, 3 to 10 µm in diameter

ZORBAX SCX 5 spherical 300

L10 Nitrile groups chemically bonded to porous silica particles, 3 to 10 µm in diameter

ZORBAX CNZORBAX SB-CNZORBAX Eclipse XDB-CN

53.5, 53.5, 5

7080, 30080

L11 Phenyl groups chemically bonded to porous silica particles, 1.5 to 10 µm in diameter

ZORBAX Eclipse XDB PhenylZORBAX Eclipse Plus Phenyl-HexylZORBAX PhenylPoroshell 120 Phenyl-HexylPursuit XRs DiPhenylPursuit DiPhenyl

51.8, 3.5, 53.52.73, 5, 103, 5, 10

709580120100200

L13 Trimethylsilane chemically bonded to porous silica particles, 3 to 10 µm in diameter

ZORBAX TMS 5 70

L14 Silica gel having a chemically bonded, strongly basic quaternaryammonium anion-exchange coating, 5 to 10 µm in diameter

ZORBAX SAXIonoSpher A

55

70120



(Continued)

usP Designations


Particle size(µm)

Pore size(Å)

L21 A rigid spherical styrenedivinylbenzene copolymer, 5 to 10 µm in diameter

PLRP-S 3, 5, 8, 10, 10-15, 15-20, 50

100

PLRP-S 3, 5, 8, 10, 10-15, 15-20, 50

300

PLRP-S 5, 8, 10, 30, 50 1000PLRP-S 5, 8, 10, 30, 50 4000PLgel 3, 5, 10, 20 50, 100, 500,

103, 105,105, 106,MIXED

L22 A cation-exchange resin made of porous polystyrene gel with sulfonic acid groups, about 10 µm in size

Hi-Plex H 8 N/A

L25 Packing having the capacity to separate compounds with a MW rangefrom 1,000 to 5,000 da (as determined by the polyethylene oxide),applied to neutral, anionic and cationic water-soluble polymers. Apolymethacrylate resin base, crosslinked with polyhydroxylated ether(surface contained some residual carboxyl functional gruops) was found suitable

PL aquagel-OH 5, 8 30

L33 Packing having the capacity to separate dextrons by molecular size over a range of 4,000 to 500,000 da. It is spherical, silica-based, and processed to provide pH stability

ZORBAX GF-250 4 150Bio SEC-3 3 100, 150,

300Bio SEC-5 5 100, 150,

300, 500,1000, 2000

ProSEC 5 300

346


L34 Strong cation-exchange resin consisting of sulfonated cross-linkedstyrene-divinylbenzene copolymer in the lead form, about 9 µm indiameter

Hi-Plex Pb 8 N/A

L35 A zirconium-stabilized spherical silica packing with a hydrophilic (diol-type) molecular monolayer bonded phase having a pore size of 150Å

ZORBAX GF-250ZORBAX GF-450

46

150, 300

L43 Pentafluorophenyl groups chemically bonded to silica particles by apropyl spacer, 5 to 10 µm in diameter

Pursuit PFP 3, 5 200

L45 Beta cyclodextrin bonded to porous silica particles, 5 to 10 µm indiameter

ChiraDex Chiral 5 100

L50 Multifunction resin with reversed-phase retention and strong anion-exhange functionalities. The resin consists of ethylvinylbenzene, 55%cross-linked with divinylbenzene copolymer, 3 to 15 µm in diameter, anda surface area of not less than 350 m2 per g. Substrate is coated withquarternary ammonium functionalized latex particles consisting ofstyrene cross-linked with divinylbenzene

ZORBAX 300SCX 5 300

L52 Weak cation-exchange resin made of porous silica with sulfopropylgroups, 5 to 10 µm in diameter

IonoSpher C 5 120

L53 Weak cation-exchange resin consisting of ethylvinylbenzene, 55%crosslinked with divinylbenzene copolymer, 3 to 15 µm diameter.Substrate is surface grafted with carboxylic acid and/or phosphoric acidfunctionalized monomers. Capacity not less than 400 µEq/column

Bio SAX 3, 5, 10 300

L56 Propyl silane chemically bonded to totally porous silica particles, 3 to 10µm in diameter

ZORBAX SB-C3 3, 5 80

L57 A chiral-recognition protein, ovomucoid, chemically bonded to silicaparticles, about 5 µm in diameter, with a pore size of 120Å

Ultron ES-OVM 5 120

L58 Strong cation-exchange resin consisting of sulfonated cross-linkedstyrene-divinylbenzene copolymer in the sodium form, about 6 to 30 µmin diameter

Hi-Plex NaHi-Plex Na (Octo)

108

N/AN/A

L60 Spherical, porous silica gel, 10 µm in diameter, the surface has beencovalently modified with alkyl amide groups and endcapped

ZORBAX Bonus-RPPoroshell 120 Bonus-RPPolaris Amide-C18

1.8, 3.5, 52.73, 5

80120180


Particle size(µm)

Pore size(Å)

usP Designations



Oligo Solutions

stratospheres Dna Cartridges

StratoSpheres DNA Synthesis Cartridges make it easy to obtain high-quality synthetic DNA oligonucleotides.The high-yielding polystyrene packing delivers more full-length product than conventional controlled-poreglass supports. In addition, the hydrophobic nature of the polystyrene promotes coupling and minimizesnon-specific binding to maximize production efficiency. These high-throughput cartridges deliver veryeconomical oligonucleotide synthesis, and provide the high performance expected from macroporouspolystyrene supports. StratoSpheres DNA synthesis cartridges deliver maximum flexibility in high-throughputenvironments.

stratospheres Dna Cartridges

Descriptionsize(nmol) Part no.

StratoSpheres DNA DMT bz dA 40 PL3554-1602dAbz200 PL3554-4602dAbz

StratoSpheres DNA DMT bz dC 40 PL3554-1602dCbz200 PL3554-4602dCbz

StratoSpheres DNA DMT ac dC 40 PL3554-1602dCac200 PL3554-4602dCac

StratoSpheres DNA DMT ibu dG 40 PL3554-1602dGibu200 PL3554-4602dGibu

StratoSpheres DNA DMT dmf dG 40 PL3554-1602dGdmf200 PL3554-4602dGdmf

StratoSpheres DNA DMT dT 40 PL3554-1602dT200 PL3554-4602dT

• Greater yields of full length products than controlled-pore glass• Inert support prevents side reactions and improves quality of the end product• 1000Å pore size permits synthesis of longer oligonucleotide sequences, up to 70-mer• Certificate of Analysis offered for every batch

StratoSpheres DNA Cartridges

348


toP, toP-Dna and toP-rna Cartridges• Superior yield and purity come from proprietary polymeric resins and optimized buffers• Typical yield is more than 85% and typical purity is over 90%, eliminating the need for multiple

sample-loading steps• Agilent TOP cartridges use up to two thirds less reagent than products from other vendors

• Fast throughput improves production efficiency• Pre-HPLC "sample prep" ability maximizes utility• Gravity (TOP) or vacuum flow (TOP-DNA) ensures flexibility

TOP-DNA is a high-throughput, simple, fast, cost-effective solution that purifies oligos up to 150-mer in length. Its high binding capacity can purify DNA oligos from 200 nmol to 1 µmol synthesis scales. TOP-DNA can also be used for sample preparation before HPLC purification for very high quality oligos in large-scale analysis. The proprietary polymeric resin is compatible with direct loading of AMAdeprotected oligo solutions.

TOP, TOP-DNA and TOP-RNA cartridges provide a high-throughput, simple, cost-effective solution for DNA and RNA oligonucleotide purification. The TOP product range incorporates a unique 96-well plate with removable tubes, streamlined gravity flow or vacuum procedure, and proprietary polymeric resin.Agilent's innovative technology delivers superior yield and purity for standard oligos up to 1 µmol synthesisscale and up to 150-mer in length. Flexibility is assured from a choice of simple gravity flow (for walk-awayand low initial setup cost) or vacuum procedure (for fast turnaround – less than 15 minutes for the entirepurification process). Up to 10 minutes drying time between each step is permissible with no effect onpurification results (drying time after the acetonitrile conditioning step should be kept to a minimum).

TOP, TOP-DNA and TOP-RNA Cartridges

TOP and TOP-DNA Cartridges

For more information on TOP RNA, view this Application Note on-line: High Performance RNA oligonucleotide purification using Agilent TOP-RNA (publication # 5990-8974EN), www.agilent.com/chem/library

tiPs & tooLs



TOP-RNA Cartridges

• A complete solution for RNA oligo purification to enhance productivity• High throughput and automation friendly, freeing up operator time• Less reagent use reduces operating costs

toP, toP-Dna and toP-rna Cartridges

Descriptionsorbent

mass (mg)Volume

(mL) unit Part no.TOP-RNA well plate tubes for 1 µmol scale 100 1.8 96/pk 7573915CTOP-RNA well plate tubes for 1 µmol scale 100 1.8 20 x 96/pk 7573915BTOP-DNA well plate tubes for 1 µmol scale 150 1.8 96/pk 7572915CTOP cartridge 500 6 30/pk 12102301TOP cartridge 300 6 30/pk 12102300Mega Bond Elut TOP 3 g 20 20/pk 14251921TOP-DNA well plate tubes for 1 µmol scale 150 1.8 20 x 96/pk 7572915BTOP well plate tubes for 50 nmol scale 25 1.8 96/pk 75719025TOP well plate tubes for 200 nmol scale 50 1.8 96/pk 75719050TOP well plate tubes for 200 nmol scale, high capacity

100 1.8 96/pk 7571901C

96-well plate sealing mat 50/pk 5133005Disposable waste tray 25/pk 5133001TOP reusable base plate 75400001VersPlate Base Plate 100/pk 75700001

With TOP-RNA you can purify short and long RNA oligos, siRNA to 21-mer and long RNA to 60-80-mer.The high binding capacity purifies RNA oligos up to 1 µmol. The proprietary polymeric resin and validatedprotocol allow deprotection of 2'hydroxyl group without removal of the 5'trityl group.

350

CoLUMNS for BioMoLeCULe SePArATioNS

LC and LC/MS Columns for BiomoleculesTable of Contents

Biocolumn Selection Guidelines .....................................351Biomolecule Separations .................................................353UHPLC/HPLC Techniques ................................................364

Reversed-Phase HPLC ......................................................365ZORBAX 300Å StableBond ..............................................367ZORBAX 300Å Extend-C18...............................................376Poroshell 300 ......................................................................380Poroshell 120 ......................................................................385PLRP-S .................................................................................387ZORBAX Amino Acid Analysis (AAA) Columns and Supplies ......................................................394Ion-Exchange Chromatography .......................................397Agilent Bio MAb HPLC Columns ....................................399Agilent Bio IEX HPLC Columns .......................................402PL-SAX Strong Anion-Exchange Columns ....................406PL-SCX Strong Cation-Exchange Columns....................410Agilent Bio-Monolith Ion-Exchange HPLC Columns....................................................................412Size Exclusion Chromatography......................................416Agilent Bio SEC-3 ..............................................................418Agilent Bio SEC-5 ..............................................................424ProSEC 300S .......................................................................428ZORBAX GF-250 and GF-450 Gel Filtration Columns ......................................................431Affinity Chromatography ..................................................434Agilent Bio-Monolith Protein A HPLC Columns...........434Agilent Protein Fractionation System and Proteomics Reagents ................................................437Multiple Affinity Removal System ..................................438Multiple Affinity Removal System Starter Kits.............441mRP-C18 High-Recovery Protein Columns....................442

Method Development........................................................444ZORBAX Column Methods...............................................444Reversed-Phase LC/MS Methods..................................446Bio Ion-Exchange Column Methods...............................447SEC Column Methods .......................................................449High Sensitivity Capillary Column Methods..................451

Capillary and Nano Columns ...........................................4522-D LC/MS Analyses Using ZORBAX Capillary and Nano LC Columns......................................456ZORBAX Bio-SCX Series II...............................................458

MicroBore (1.0 mm id) Columns.....................................461Purification – Prep HPLC..................................................464ZORBAX PrepHT ................................................................466PLRP-S for Prep to Process..............................................467PL-SAX and PL-SCX for Prep to Process.......................472Peptide Purification ...........................................................475VariTide RPC Columns for Synthetic Peptides .............475VariPure IPE ........................................................................476

Appendices.........................................................................477BioHPLC Columns Literature ...........................................477ZORBAX 300 Citations ......................................................485Poroshell 300 Citations.....................................................486PLRP-S Citations ................................................................486PL-SAX Citations................................................................487PL-SCX Citations................................................................487

351www.AGiLeNT.CoM/CHeM/LC


Agilent has complete solutions for your needs. These include the Agilent 1260 Infinity Bio-inert LC systemwith a metal-free sample path and the Agilent 1290 Infinity LC, designed to provide highest speed,resolution, and ultra-sensitivity for UHPLC applications, including those utilizing Agilent wide-pore 300ÅZORBAX StableBond columns. Biomolecules may be complex in structure, but their analysis is simplified by using Agilent HPLC columns, systems, and supplies.

What is a biomolecule?

Proteins – separation based on size with size exclusion chromatography, charge with ion-exchangechromatography, and hydrophobicity with reversed-phase chromatography.

Peptides – biocolumns for the analysis and purification of the full range of peptides, including hydrophobic,hydrophilic, basic and acidic peptides across the full size range. Also, columns for peptide mapping by HPLCand UHPLC.

DNA/rNA oligonucleotides – reversed-phase and ion-exchange options for DNA and RNA oligos, and with particle pore sizes to cover the full range of oligonucleotide sizes, from small synthetic oligos tolarge plasmids.

Amino acids – the ZORBAX Eclipse Amino Acid Analysis HPLC columns provide a high efficiency solutionfor rapid analysis of 24 amino acids. Typical analysis times range from 14 minutes, with a 75 mm column, to 24 minutes with a 150 mm column.

Broad-distribution polymers – analysis of lipids, polysaccharides and drug delivery compounds using polymeric columns and standards to determine their molecular weight distribution and composition. These compounds tend to exhibit broad MW distributions, in contrast to other biomolecules that havenarrow MW distributions or a defined molecular weight.

From sample purification to analysis, Agilent's biomolecule columns and supplies are easy to integrate intoyour workflow for a complete, reproducible, and high-quality solution.

In this section of the catalog you will also find advice and tips on solvent choice, mobile phase modification,optimization, and example separations to assist you in column selection and method development.

In this section, we deal with the separation of:

Biomolecules are compounds made by living organisms. They can range in size from amino acids and smalllipids to large polynucleotides such as DNA or RNA.

352


What is a biocolumn? Biochromatography columns, or biocolumns, are liquid chromatography columns used for the separation of biological compounds such as peptides and proteins, oligonucleotides and polynucleotides, and otherbiomolecules and complexes. Biocolumns are specifically designed for biomolecule analysis with larger pore sizes to accommodate the larger molecule sizes. Media is designed to minimize non-specific binding of analytes for improved recovery. Separation mechanisms are chosen to either retain biological function so bioactivity is not lost during analysis, or to deliberately denature for primary structure characterization.

Typically, HPLC has been used to separate biomolecules. Now, advanced techniques such as UHPLC arebecoming a popular choice because multiple separation mechanisms are needed in the characterization ofbiomolecules. Therefore, Agilent offers advanced chemistries developed specifically for the separation ofbiomolecules using size exclusion, reversed-phase, ion-exchange, and affinity functionalities, all of which arecovered in this section of the catalog.



Proteins are complex molecules that require multiple techniques to provide full characterization. They exist as three-dimensional structures and it is thisstructure that confers their biological activity.

The sequence of the amino acid chains defines the primary structure of the protein. Hydrogen bonding between amino acids of the primary structure thenconfers a secondary structure typically in the form of alpha helices and pleated sheets. A further series of interactions, hydrogen bonding, ionic, hydrophobicand disulphide bridges, between regions of the secondary structure, then provides the tertiary protein structure, or three-dimensional conformation. If theprotein is composed of a number of amino acid chains, the interaction between these chains gives the quaternary structure.

When looking at methods for protein characterization, it is therefore clear from Figure 1 that techniques will be required that characterize the protein in itsnative state, without disrupting the tertiary and quaternary structures. We also need techniques for assessing the primary amino acid sequence, in the fullydenatured state with the three-dimensional structure stripped away.

Hydrogen bonds

Pleated sheet Secondary protein structure

occurs when the sequence of amino acids are linked by hydrogen bonds

Tertiary protein structureoccurs when certain attractions are present between alpha helices and pleated sheets

Quaternary protein structureis a protein consisting of more than one amino acid chain

figure 1. Schematic showing the various levels of protein structure.

Hydrogen bondsIonic interactionsHydrophobic interactionsDisulphide bridges

Primary protein structureis a sequence of amino acids

Amino acids

Alpha helix

Pleated sheet

Alpha helix

The environment of the protein can influence, stabilize, or disrupt the structure of the protein. Factors to consider include pH, temperature, saltconcentrations, aqueous or organic solvent content, and for some proteins, the presence of a stabilizing small molecule or metal ion. Protein structure can also be disrupted by the use of sulfhydryl reducing agents to break -S-S- bonds or chaotropic agent, like urea or guanidine HCI. With the complexity of proteins and the intramolecular interactions that determine the three-dimensional structure, you can also expect that there will be intermolecularassociations between protein molecules and other molecular entities and the surfaces with which they come into contact. This can result in proteincomplexes, aggregation (with possible precipitation), and deposition on surfaces, including those of the HPLC column and system. Therefore, you should consider the handling and environment in which the protein is maintained.

Protein Separations

354


Application Technique Agilent Columns Notes

Primary structureanalysis

UHPLC/HPLCreversed-phaseseparations

ZORBAX 300SBPoroshell 300SBPLRP-S

Reversed-phase separations require (or cause) denaturing of the protein to obtaindetailed information about the amino acid sequence and/or amino acid modifications(including post-translational modifications).

Aggregationanalysis

Size exclusionseparations

Bio SEC-3Bio SEC-5ProSEC 300SZORBAX GF

Aggregates in protein biopharmaceuticals are of major concern as they can induce animmunogenic response and can influence the composition of the final formulation.

Charge variantanalysis

Ion-exchangeseparations

Agilent Bio IEXAgilent Bio MAbPL-SAXPL-SCX

The ratio of individual amino acids determines the net charge of the protein molecule.The pH at which the net charge is zero is called the isoelectric point (pI). When thesolution pH is less than the pI, the protein will be positively charged (acidic), and whenthe solution pH is greater than the pI, the protein is negatively charged (basic). For ion-exchange analysis, we recommend the eluent pH be at least one pH unit away from its pI. Protein analysis using ion-exchange columns requires bufferedmobile phase and either salt gradients or pH gradients for elution.

Protein Column Selection Guide

min

mAU

0

2.5

5

7.5

10

12.5

15

17.5

0.14

8

1.38

4

1.64

8

Higher resolution of oxidation studyColumn: ZorBAX rrHD 300SB-C18

857750-9022.1 x 50 mm, 1.8 µm

Mobile Phase: A: 0.1% TFAB: 0.01% TFA + 80% ACN


Gradient: 33 to 50% B, 0 to 4 min

Detector: 1290 Infinity LC with diode array detector at 280 nm

Sample: Insulin, insulin chain A and chain B, oxidized (bovinesigma, 1 mg/mL)

oxidized insulin chain A

oxidized insulin chain B

insulin

Subspecies of oxidized insulin chain B

It is evident that the oxidized insulin chains are resolved from insulin in under 2 minutes using the Agilent ZORBAX RRHD 300SB-C18 2.1 x 50 mm, 1.8 µm column.



intact MAb monomer and dimer separationColumn: Bio SeC-3, 300Å

5190-25117.8 x 300 mm, 3 µm

Buffer: Sodium phosphate buffer, pH 7.0, 150 mM

Isocratic: 0-100% Buffer A from 0-30 min


Sample: CHO-humanized MAb, 5 mg/mL – intact

Injection: 5 µL

Detector: UV 220 nm


VLC_MD_Mab

0

50

100

150

200

250

300

mAU

4 6 8 10 12 14 min

Monomer

Dimer

10 10.5 11 11.5 12 12.5 13 13.5 14 14.5 min0

10

20

30

40

50mAU

Separation of charge variants of human igG1with pH gradientColumn: Agilent Bio MAb

5190-24112.1 x 250 mm, 5 µm

Mobile Phase: A: 10 mM Na2HPO4, pH 6.0B: A + 0.5 M NaCl or just 0.5 M Na2HPO4, pH 6.0

Flow Rate: 2 mL/min

Gradient: 0.5 min hold with mobile phase A followed by a lineargradient to 45% B in 15 min (elapsed time 15.5 min);then 60% B at 15.6 min continued to 20 min. Column flushed with 100% B for 15 min before re-equilibration for the next run.pH Gradient: A: 5 mM Na2HPO4, buffer pH 5.5 and B: 40 mM NA2HPO4 (not buffered, pH 8.9). 2% B/min at 1 mL/min for 15 min, followed by a column wash with 90% B for 5 min.

Detector: UV at 220 nm

Sample: One mg each/mL in mobile phase AMonoclonal antibodies (MAb) -human IgG1 (5 mg/mLstock solution) derived from CHO cells

Instrument: Agilent 1200 SL system with diode array detector

Before carboxypeptidase B digestionAfter carboxypeptidase B digestion

MAb c-terminal cleavage: Human IgG1 MAb, 1 mg/mL in 25 mM Na2HPO4 buffer, pH 7.5, was incubated with approximately 25 units of thecarboxypeptidase B for 18 hours and 10 µL samples were injected.

356


Peptide Separations

Peptide mapping is required for the characterization of proteins. It is used to confirm the identity of a proteinand to identify and quantify post-translational modifications.

The purified protein is first digested using an enzyme, such as trypsin, yielding a range of peptide fragments.The specificity of the enzyme cleavage produces a fingerprint of peptides which is characteristic of thatprotein. Identification of the peptide fragments confirms the identity of the protein, and changes in theprofile of the peptide digest can be used to identify post-translational modifications to that protein that may have occurred during the manufacturing or purification processes.

Reversed-phase UHPLC/HPLC is the preferred technique for the analysis of peptide digests with either MS or UV detection. LC/MS is used for the identification of the peptide fragments and determination of sequence coverage whereas LC/UV is more commonly used for peptide map comparisons in themonitoring/QC segments. To achieve sufficient resolution for quantification and identification, longer columnlengths or higher efficiency particles such as the sub-2 µm ZORBAX RRHD, or superficially porous Poroshellare recommended.

Peptide digests are complex mixtures, and for complete coverage, i.e. resolution of the individual peptides, a high efficiency/high resolution column is required. The peptide fragments can range in size andhydrophobicity, so Agilent offers several columns for peptide mapping. There are three options: pore sizes,particle sizes, and superficially porous and fully porous for UHPLC separations.

Peptide Mapping

TiPS & TooLS

Capillary electrophoresis is an alternative technique to liquid chromatography for the separation of complex peptide mixtures. Further informationcan be found in the following Case Study:

An orthogonal view of peptide mapping – analysis of bovine serum albumin digest using capillary electrophoresis and quadrupole time-of-flightmass spectrometry (publication # 5990-7631EN)

www.agilent.com/chem/library



Peptide Mapping Column SelectionRecommended column choices determined by system/column pressure maximum and peptide size/hydrophobicity.

increased resolution for peptide mappingColumn: ZorBAX 300SB-C18

858750-9022.1 x 100 mm, 1.8 µm



Gradient: 2% B for 1 min, 2 to 45% B for 8.8 min, 45 to 95% Bfor 0.2 min, 95% B for 2 min, 95 to 2% B for 0.2 min

Temperature: 50 °C


Sample: Enzymatic protein digest (MAb)

Norm350

300

250

200

150

100

50

0

1 2 3 4 5 6 7 8 9 min

-50


Large peptidefragments/hydrophobicpeptide core

400 bar HPLC Poroshell 300 SB-C18ZORBAX 300SB-C18, 3.5 µm

Agilent 1200 Infinity LC

600 bar UHPLC Poroshell 300 SB-C18 Agilent 1260 Infinity LC and 1260 Infinity Bio-inert Quaternary LC1200 bar UHPLC ZORBAX RRHD 300SB-C18,

1.8 µm Poroshell 300 SB-C18


Small hydrophobicpeptides

400 bar HPLC Poroshell 120 EC-C18Poroshell 120 SB-C18


600 bar UHPLC Poroshell 120 EC-C18Poroshell 120 SB-C18

Agilent 1260 Infinity LC and 1260 Infinity Bio-inert Quaternary LC



If you have an Agilent 1290 Infinity LC in your lab, we recommend starting with a ZORBAX RRHD 300SB-C18 column to screen your peptide map.

The longer 100 mm Agilent ZORBAX RRHD 300SB-C18 column provides maximum resolution for protein digests – in this sample the total run time,including washing and equilibration, is under fifteen minutes.

358


Separation of Natural and Synthetic PeptidesPurification columns and media are required for the isolation and analysis of natural and synthetic peptides. Purity and recovery determination of the isolated or purified peptide requires the use of highefficiency columns. The primary technique used for the isolation and purification, and analysis, is reversed-phase HPLC.

The fractions from a purification or isolation workflow and the final peptide product are analyzed for purity using high efficiency columns. The peptides will vary in size, charge and hydrophobicity and so, as with peptide mapping applications, Agilent offers a range of columns to provide optimum separations of the full range of peptides. For small peptides, typically less than 10 amino acid residues, the smaller pore UHPLC materials are used, but if the peptide is larger, contains more amino acid residues, or exists in a dimeric or multimeric form, then the larger pore size 300Å columns provide better separations due toimproved mass transfer.

Natural and Synthetic Peptides Column SelectionRecommended column choices as determined by system/column pressure maximum for the analysis ofnatural and synthetic peptides.


Larger peptides with more than 10 amino acid residues

400 bar HPLC Poroshell 300 SB-C18ZORBAX 300SB-C18, 3.5 µmPLRP-S


600 bar UHPLC Poroshell 300 SB-C18 Agilent 1260 Infinity LC and 1260 Infinity Bio-inert Quaternary LC1200 bar UHPLC ZORBAX RRHD 300SB-C18, 1.8 µm Agilent 1290 Infinity LC

Peptides with typicallyless than 10 aminoacid residues

400 bar HPLC Poroshell 120 EC-C18Poroshell 120 SB-C18PLRP-S



Agilent 1260 Infinity LC and 1260 Infinity Bio-inert Quaternary LC

Reversed-phase columns are also the first choice for purifying large numbers of individual peptides or largeramounts of a particular peptide. High efficiency, small particle pre-packed prep columns are available forthe high efficiency purification of small amounts of peptides, and larger particle columns and bulk media forthe larger scale purifications, as shown in Table 1.



Table 1. Agilent columns for small- to large-scale peptide purifications.

Agilent Column

Amount of Peptide required

mg g kgZORBAX Prep HT 300StableBondVariTide RPCPLRP-S

After solid phase synthesis (SPS) using a polystyrene resin such as one of the Agilent StratoSpheresproducts, the peptide is cleaved from the support and the resultant mixture is separated to obtain the targetpeptide. A high efficiency column is needed for the purification as the candidate peptide must be resolvedfrom peptides that are very similar in structure. Check www.agilent.com for further information.

Preparative scale purification of Leuprolide by concentration overloadColumn: PLrP-S 100Å, 10 µm

PL1412-4100Bulk Media: Load & Lock 4001 Column

PCG93LL500X25Mobile Phase: Isocratic separation

using 0.1% TFA in 28% ACN:72% water

Flow Rate: Linear velocity 360 cm/hr

0 Time (min) 40

Crude leuprolide separation of 30 mg on-column load.

% Purity (Pre-impurity 1)

% Purity (Leuprolide)

% Purity (Post-impurity)

Fraction analysis – the concentration overload purification.

360


DNA and RNA Oligonucleotide SeparationsThere is a renewed interest in oligonucleotides (oligos) as they are used in more and more applications,including potential therapeutics. The synthesis workflow is similar to that used for the more establishedsynthetic peptide production, i.e. an activated solid phase synthesis resin is used with sequential addition of specific nucleotides to build the desired sequence.

The nucleotide building blocks are protected at the 5’ hydroxyl end with a dimethoxytrityl (DMT) group andthe cleaved target oligo will have this protected group still attached. As DMT is hydrophobic, it is a usefulhandle that can be used for the first stage step. To increase the stability of the oligonucleotide, particularly toenzyme degradation, it may be chemically modified, for example by replacing oxygen with sulfur to producephosphorothioates.

When using chemical synthesis to produce biomolecules, the coupling efficiency of each additional cycle is never 100%. The sample, after cleavage from the solid phase synthesis support, will contain deletionsequences, oligos where one or more residues are missing, and some amount of larger oligos produced bydouble coupling or branching. The sample mixture is complex and high efficiency techniques are requiredfor analysis.

There are three UHPLC/HPLC techniques that are routinely used for oligonucleotide separations:

Trityl-on: This procedure is relatively simple to perform and separates the full-length target oligo, which stillhas the DMT group attached, from the deprotected failure sequences. The analytical information obtained is limited and this is generally considered to be a purification method.

ion-exchange separations of the trityl-off, deprotected oligos: This method uses the negativecharge on the backbone of the oligo to facilitate the separation. Resolution is good for the shorter oligos butdecreases with increasing chain length. Aqueous eluents are used but oligos are highly charged, and highconcentrations of salt are needed to achieve elution from the column.

ion-pair reversed-phase separation of the trityl-off, deprotected oligos: This technique usesorganic solvents and volatile ion-pairing agents and is suitable for LC/MS. The technique is best performedwith high efficiency particles. Conditions that fully denature the oligos and prevent association withcomplimentary sequences are required. Thus, the separation is best performed at elevated temperatures.



DNA and RNA Oligonucleotide Column Selection

TiPS & TooLS


Trityl-on/trityl-offoligonucleotides

Trityl-on PLRP-S 50 µm media Separates due to differences in hydrophobicity. Ideal for the separation of trityl-on from trityl-off oligos and is also used for ion-pair reversed-phaseseparations of deprotected oligos.Deprotected

oligonucleotidesIon-pair reversed-phaseseparation of the trityl-off,deprotected oligos

PLRP-S 3 µm to 50 µm

Deprotectedoligonucleotides

Ion-exchange separationsof the trityl-off,deprotected oligos

PL-SAX 1000Å Separates deprotected oligos under denaturing high pH conditions. The quaternary amine functionality on the polymeric particles enables ion-exchange separations at high pH, improving chromatography for self-complementary sequences.

Further information can be found in the following publications:Agilent PLRP-S 100Å HPLC Columns and Media (publication # 5990-8187EN)Agilent PL-SAX 1000Å HPLC Columns and Media (publication # 5990-8200EN)www.agilent.com/chem/library

362


Amino Acid Analysis

ZorBAX eclipse AAA Column Selection

Application Diameter x Length (mm) Particle Size (µm)Analytical routine sensitivity 4.6 x 150 5.0Analytical routine sensitivity, high-resolution using FLD 4.6 x 150 3.5Analytical routine sensitivity, high-throughput 4.6 x 75 3.5Solvent Saver high sensitivity, high-resolution 3.0 x 150 3.5

Ser

Serine

S105.0987.08C 3 H7 NO3

His

Histidine

H155.16137.14C6H 9N 3 O 2

Arg

Arginine

R174.20156.19C6 H14 N 4O 2

Lys

Lysine

K146.19128.17C6H14 N 2O2

Ile

Isoleucine

I131.18113.16C6H13NO 2

Phe

Phenylalanine

F165.19147.18C9H11NO 2

Leu

Leucine

L131.17113.16C 6H13NO2

Trp

Tryptophan

W204.23186.21C11H12 N 2 O2

Ala

Alanine

A89.0971.08C3H 7NO2

Met

Methionine

M149.21131.20C5H 11NO 2 S

Pro

Proline

P115.1397.12C5H 9NO 2

Cys

Cysteine

C121.16103.14C3H7 NO 2S

Asn

Asparagine

N132.12114.10C4H8N 2O3

Val

Valine

V117.1599.13C 5H 11NO2

Gly

Glycine

G75.0757.05C 2H 5NO 2

Ser

Serine

S105.0987.08C3H 7NO3

Gln

Glutamine

Q146.15128.13C 5H 10 N 2O 3

Tyr

Tyrosine

Y181.19163.17C9H 11NO 3

Asp

Aspartic Acid

D133.10115.09C 4H 7NO4

Glu

Glutamic Acid

E147.13129.11C 5H 9NO 4

Thr

Threonine

T119.12101.10C 4H 9NO 3

Chart of the Amino Acids

Basic

Nonpolar (hydrophobic)

Polar, uncharged

Acidic

1-Letter Amino Acid CodeMolecular WeightMW-H2OMolecular Formula

3-Letter Amino Acid Code

Chemical Structure

Chemical Name

Agilent offers several good options for separation of amino acids, including the Agilent ZORBAX Eclipse AAAcolumn which uses an updated protocol and is specially tested using amino acids. The ZORBAX Eclipse AAAhigh efficiency column rapidly separates amino acids following an updated and improved protocol. Total analysis from injection to injection can be achieved in as little as 14 min (9 min analysis time) on shorter, 7.5 cm columns and 24 min (18 min analysis time) on the 15 cm column. Exceptional sensitivity(5 to 50 pmol with diode array or fluorescence detectors) and reliability are achieved using both OPA- and FMOC-derivatization chemistries in one fully automated procedure using the Agilent 1200 Infinity LC.The newer ZORBAX Eclipse Plus C18 column is also an excellent choice for amino acid separations.

For more information on the ZORBAX Eclipse Plus C18 column, turn to page 248.



Broad Distribution Biomolecules

Carbohydrates, Lipids and PEGsAqueous size exclusion chromatography employing columns packed with polymeric media can be extremelyuseful when investigating biomolecules and their derived species with broad molecular weight distributions.Examples include PEGylated proteins and complex polysaccharides which find use in biopharmaapplications. The wide pore size distribution of polymeric SEC columns compared to silica-based materialare excellent for samples with polydispersities greater than one.

Broad Distribution Biomolecule Column Selection

Low MW polymers and oligomers,oligosaccharides, PEGs,lignosulfonates

2 or 3 PL aquagel-OH columns The PL aquagel-OH analyticalseries has a pH range of 2-10,compatible with organic solvents(up to 50% methanol),mechanical stability up to 140 bar(2030 psi) and low columnoperating pressures.

ü PL aquagel-OH 8 µmü PL aquagel-OH 20 5 µmü PL aquagel-OH MIXED-M 8 µm

Polydisperse biopolymers,polysaccharides, cellulosederivatives

2 or 3 PL aquagel-OH columnsü PL aquagel-OH MIXED-H 8 µmü PL aquagel-OH 60/50/40 8 µm

Very high MW polymers,hyaluronic acids,starches, gums

PL aquagel-OH 60/50/40 15 µm in series

364


UHPLC/HPLC TechniquesHigh-performance liquid chromatography, HPLC, is a chromatographic technique that can separate a mixture of compounds and is used in biochemistry and analytical chemistry to identify, quantify and purify the individual components of the mixture. There has been an evolution toward ultra high-performanceliquid chromatography (UHPLC) which is widely accepted for high-efficiency separations of small- to medium-sized molecules, and has been used to reduceanalysis time and/or to increase resolution. The use of UHPLC has been extended to large biomolecules with the introduction of wide pore chromatographicmedia in columns that can withstand pressures of 600 to 1200 bar.

On the following pages you will see the wide range of columns that Agilent offers for the HPLC and UHPLC separation of proteins and other biomolecules.

UHPLC/HPLC Techniques for Biomolecule Analysis

Technique Advantages DisadvantagesReversed-Phase ü High resolution

ü High capacityü Relatively simpleü Sample concentrated on-columnü Small particle, 1.8 µm, for UHPLC separationsü Polymeric media for unsurpassed chemically and thermally stable

ü Denaturing conditionsü High efficiency silica columns cannot be cleaned using aggressive

solvents when performing purifications

Ion-Exchange ü Good recovery of biological activityü High capacityü Sample concentrated on-column

ü Limited MS compatibility due to presence of salts

Size Exclusion ü Good recovery of biological activityü Non-interactive technique with good sample recovery

ü No sample concentrationü Limited capacity

Affinity ü Highly selectiveü Good recovery of biological activityü Sample concentrated on-columnü Often single step isolation

ü No sample concentrationü Limited capacity



reversed-Phase HPLCConfidently perform high-resolution separationsReversed-phase UHPLC/HPLC separates solutes based on differences in hydrophobicity, with the leasthydrophobic peak eluting first. This high-resolution technique is capable of separating peptides, proteins and oligonucleotides that differ by only one amino acid or nucleotide residue.

Because HPLC uses organic solvents (such as acetonitrile, methanol, ethanol and propanol) it is also adenaturing technique that disrupts a biomolecule’s three-dimensional structure. This allows you to obtaininformation about a molecule’s primary structure and sequence, as well as variations in the sequence to be identified.

Agilent offers the industry’s broadest range of wide-pore reversed-phase columns, all backed by technical support experts and application chemists around the globe. This section features the followingcolumn innovations:

• ZorBAX 300Å pore silica columns – an industry first for reversed-phase protein and biomoleculeseparations – are available in 6 phases, along with a broad array of sizes. For fast UHPLC separations,we also offer a 1.8 µm particle size option that withstands pressures up to 1200 bar, and can be usedwith high-pressure instruments, such as Agilent’s 1290 Infinity LC.

• Agilent Poroshell columns feature the industry’s first solid core/porous shell particle. Our wide-porePoroshell 300 columns are ideal for fast chromatography, and are available in a variety of phases.

• Agilent PLrP-S columns contain polymer particles, and can be used to separate peptides andproteins of various sizes and DNA/macromolecular complexes. These columns are unique in that theyare 100% organic, can withstand temperatures as high as 200 °C, and can be used under conditionsfrom pH 1 to pH 14.

• Choose from a range of column sizes, particle sizes (3-8 µm for analytical separations) and pore sizes(100Å to 4000Å). Preparative columns (10-50 µm) are also available, either prepacked in columns oras bulk material.

366


reversed-Phase Column Selection

Application Agilent Columns NotesProteins and polypeptides ZORBAX 300Å, 1.8 µm Improved packing processes achieve stability up to 1200 bar for use with the Agilent

1290 Infinity LC. RRHD 1.8 µm columns are available in 50 and 100 mm lengths forfast or high resolution – truly high definition – separations of the most complexsamples.

ü RRHD 300SB-C18ü RRHD 300SB-C8ü RRHD 300SB-C3ü RRHD 300-Diphenylü RRHD 300-HILICZORBAX 300Å StableBond Wide-pore, 300Å columns are necessary for an efficient separation of proteins and

peptides, or other large molecules, to allow these analytes to completely access thebonded phase. C18 and C8 are ideal for complex protein and protein digestseparations. StableBond provides enhanced stability for low pH.

ü 300SB-C18ü 300SB-C8ü 300SB-C3ü 300SB-CNZORBAX 300Å Extend-C18 Incorporate a unique patented bidentate silane, combined with a double-

endcapping process that protects the silica from dissolution at high pH – up to pH 11.5.

Peptides and proteins up to 1,000 kDA, monoclonal antibodies and intact proteins

Poroshell 300 Poroshell columns use a unique particle made with a layer of porous silica on a solidcore of silica. This reduces the diffusion distance for proteins making practical, rapidHPLC separations of peptides and proteins.ü 300SB-C18

ü 300SB-C8ü 300SB-C3ü 300Extend-C18

Small hydrophilic peptides in protein digests

Poroshell 120 The 120Å pore size is ideal for the fast high resolution analysis of small hydrophilicpeptides and peptide fragments in protein digests.

Peptides to DNA PLRP-S Particles are inherently hydrophobic so an alkyl ligand bonded phase is not requiredfor reversed-phase separations. This gives a highly reproducible material that is freefrom silanols and heavy metal ions.ü 100Å

ü 300Åü 1000Åü 4000Å

Small molecules/peptides/oligonucleotides PLRP-S 100ÅRecombinant peptides/proteins PLRP-S 300ÅLarge proteins PLRP-S 1000ÅDNA/high speed separation PLRP-S 4000Å




SurfaceArea

TempLimits*

pHrange* endcapped

CarbonLoad

ZORBAX 300SB-C18 300Å 45 m2/g 90 °C 1.0-8.0 No 2.8%ZORBAX 300SB-C8 300Å 45 m2/g 80 °C 1.0-8.0 No 1.5%ZORBAX 300SB-C3 300Å 45 m2/g 80 °C 1.0-8.0 No 1.1%ZORBAX 300SB-CN 300Å 45 m2/g 80 °C 1.0-8.0 No 1.2%ZORBAX 300-Diphenyl 300Å 45 m2/g 80 °C 1.0-8.0 Yes 1.9%

Specifications represent typical values only*300StableBond columns are designed for optimal use at low pH. At pH 6-8, highest column stability for all silica-basedcolumns is obtained by operating at temperatures <40 °C and using low buffer concentrations in the range of 0.01-0.02 M.At mid or high pH, 300Extend-C18 is recommended.


ZorBAX 300Å StableBond

Sterically Protected 300StableBond Bonded Phase

TiPS & TooLS

Agilent ZORBAX 300Å StableBond columns are an ideal choice for the reproducible separations of proteinsand peptides for two key reasons. First, wide-pore, 300Å columns are necessary for an efficient separationof proteins and peptides, or other large molecules, in order to allow these analytes to completely access thebonded phase. Second, 300StableBond columns are unmatched in their durability at low pH, such as withTFA-containing mobile phases typically used for protein and peptide separations. For LC/MS separations at low pH, 300StableBond columns can also be used with formic acid and acetic acid mobile phasemodifiers. These columns are available in five different bonded phases (C18, C8, C3, CN, and Diphenyl*) for selectivity and recovery optimization of proteins and polypeptides. To further increase sample recoveryand improve efficiency for difficult proteins, 300StableBond columns can be used up to 80 °C. 300SB-C18and 300SB-C8 columns are an ideal choice for complex protein and protein digest separations. Thesecolumns are also available in capillary (0.3 and 0.5 mm id) and nano (0.075 and 0.10 mm id) dimensionsfor reversed-phase LC/MS separations of protein digests. Capillary and nano columns can be used for either 1-D or 2-D proteomics separations.

*Diphenyl is available in a 1.8 µm particle size only.

Further information can be found in the following publication:

Comparison of ZORBAX StableBond 300Å LC Columns to Optimize Selectivity for Antibody SeparationsUsing HPLC and LC/MS (publication # 5989-6840EN)www.agilent.com/chem/library

368


TiPS & TooLS

Typical mobile phases for protein and peptide separations combine a very low pH with TFA (or other acids) to solubilize proteins. StableBond columnshave extremely long lifetimes under these conditions. They are available in 300Å pore size for proteins up to 100-500 kDa.

Higher resolution of intact monoclonal antibodyColumn: ZorBAX rrHD 300SB-C8

857750-9062.1 x 50 mm, 1.8 µm

Mobile Phase: A: H20:IPA (98:2) + 0.1% TFA (v/v)B: IPA:ACN:H20 (70:20:10) + 0.1% TFA (v/v)

Flow Rate: Between 0.5 mL/min and 1.0 mL/min

Gradient: Multi-segmented and linear elution

Temperature: 80 °C

Detector: Agilent 1290 Infinity LC with auto injector (ALS),binary pump and thermostatted oven and diode arraydetector (DAD), UV, 225 nm

mAU250

200

150

100

500

mAU

250

350

150

500

0 2 4 6 8 10 min

0 2 4 6 8 10 min

mAU100

80

60

40

20

0 1.2 1.4 1.6 1.8 2.0 2.2 2.4 2.6 2.8 min

increased sensitivity

Expanded View

Shoulder

Gradient A0.5 mL/min

optimized resolution

Gradient B1.0 mL/min

High speed anaysis time

resolved

Higher resolution of oxidation studyColumn: ZorBAX rrHD 300SB-C18

857750-9022.1 x 50 mm, 1.8 µm



Gradient: 33 to 50% B, 0 to 4 min


Sample: Insulin, insulin chain A and chain B, oxidized(bovinesigma, 1 mg/mL)

min

mAU

0

2.5

5

7.5

10

12.5

15

17.5

0.14

8

1.38

4

1.64

8

Subspecies of oxidized insulin chain B

insulinoxidized insulin chain B

oxidized insulin chain A

It is evident that the oxidized insulin chains are resolved from insulin in under 2 minutes using the Agilent ZORBAX RRHD 300SB-C18 2.1 x 50 mm, 1.8 µm column.



improved reproducibility of monoclonal antibodiesColumn: ZorBAX rrHD 300SB-C8

857750-9062.1 x 50 mm, 1.8 µm

Mobile Phase: A: H20:IPA (98.2), 0.1% TFAB: IPA:ACN:H20 (70:20:10), 0.1% TFA


Temperature: 80 °C


Sample: MAb

Gradient timescaleTime (min) % Solvent B

0.00 253.00 354.00 905.00 25

min

0 0.5 1 1.5 2 2.5 3 min

100

200

300

400

100

300

500

700

0 5

bar750

500

250

mA

mA

1st injection150th injection

pre- and post-150 injection column blank run overlays

pressure

UVExcellent column reproducibility and proteinrecovery using Agilent ZORBAX 300SB-C8.

gradient wash and re-equilibration region

increased resolution for peptide mappingColumn: ZorBAX 300SB-C18

858750-9022.1 x 100 mm, 1.8 µm



Gradient: 2% B for 1 min, 2 to 45% B for 8.8 min, 45 to 95% Bfor 0.2 min, 95% B for 2 min, 95 to 2% B for 0.2 min

Temperature: 50 °C


Sample: Enzymatic protein digest (MAb)

Norm350

300

250

200

150

100

50

0

1 2 3 4 5 6 7 8 9 min

-50

The longer 100 mm Agilent ZORBAX RRHD 300SB-C18 column provides maximum resolution for proteindigests – in this sample the total run time, including washing and equilibration, is under fifteen minutes.

370


Peptides: effect of TfA concentrationColumn: ZorBAX 300SB-C8

883995-9064.6 x 150 mm, 5 µm

Mobile Phase: A: Water and TFAB: ACN and TFA


Gradient: 0 min 0% B30 min 30% B

Temperature: 40 °C

Detector: UV 254 nm

Sample: Peptide Standards S1-S5, decapeptides differing slightly in hydrophobicity, 6 µL

LCBP021Retention Time (min)

S1 S2 S3 S4 S5

S1 S2 S3 S4 S5

S1S2 S3 S4 S5

8 10 12 14 16 18 20 22 246

8 10 12 14 16 18 20 22 246

8 10 12 14 16 18 20 22 246

Peptide Sequence

0.05% TfA

0.25% TfA

1.0% TfA

Peptides/proteins: effect of elevatedtemperatureColumn: ZorBAX 300SB-C3

883995-9094.6 x 150 mm, 5 µm

Mobile Phase: A: 5:95 ACN:Water with 0.10% TFA (v/v%)B: 95:5 ACN:Water with 0.085% TFA (v/v%)


Gradient: 15-53% in 20 min, posttime 12 min

Temperature: Ambient – 60 °C

Detector: UV 215 nm

Sample: Polypeptides

1. Leucine Enkephalin2. Angiotensin II3. RNase A4. Insulin (BOV)5. Cytochrome c6. Lysozyme7. Myoglobin8. Carbonic anhydrase

LCBP026Time (min)

12

3

4

4, 5

5

4

5

4

5

6

7 8

42 8 10 12 14 16 18 200 6Time (min)

42 8 10 12 14 16 18 200 6

Ambient 45 °C

60 °C35 °C

TiPS & TooLS

The Agilent 1290 Infinity LC delivers significantly faster results and higher data quality – enabling more informed decisions in shorter time. This higherproductivity gives you competitive advantages and provides you a higher return on investment. Calculate for yourself how much you can save bydeploying the 1290 Infinity technology. The online method translator and cost savings calculator helps you to transfer your HPLC methods and calculateyour cost savings, at www.agilent.com/chem/hplc2uhplc



Short-chain ZorBAX 300SB-C3 is stable at lowpH, high temperatureColumn: ZorBAX 300SB-C3

883995-9094.6 x 150 mm, 5 µm

Mobile Phase: Gradients 0-100% B in 80 minA: 0.5% TFA in WaterB: 0.5% TFA in AcetonitrileIsocratic Retention Test Conditions:1-phenylheptane 50% A, 50% B


Temperature: 60 °C

LCSB005Volume of Mobile Phase (mL)

% k

Phe

nylth

epta

ne R

emai

ning

0 1,000 2,000 3,000 4,000 5,000 6,000 7,000 8,00040

50

60

70

80

90

100

ZorBAX 300 SB-C3Competitor C4

four different 300SB bonded phases optimizeseparation of large polypeptidesColumn A: ZorBAX rrHD 300SB-C18

883995-9024.6 x 150 mm, 5 µm

Column B: ZorBAX 300SB-C8883995-9064.6 x 150 mm, 5 µm

Column C: ZorBAX 300SB-C3883995-9094.6 x 150 mm, 5 µm

Column D: ZorBAX 300SB-CN883995-9054.6 x 150 mm, 5 µm

Mobile Phase: Linear Gradient, 25-70% B in 40 minA: 0.1% TFA in WaterB: 0.09% TFA in 80% Acetonitrile/20% Water


Temperature: 60 °C

Sample: 3 µg each protein

1. RNase2. Insulin3. Cytochrome c4. Lysozyme5. Parvalbumin6. CDR7. Myoglobin8. Carbonic Anhydrase9. S-100b

10. S-100a

LCSB006

1

2, 3

4 5

6

87

910

14

3

25

6, 7

8

910

14

3

25 7

68

9

10

14

3

25

7

6

8

910

Time (min)

A

B

C

D

0 5 20 25 30 35 401510

The 300SB-C18, C8, C3, and CN bonded phases all provide a different separation of thisgroup of polypeptides. This adds an important parameter for quickly optimizing proteinseparations. The 300SB-CN column offers unique selectivity for more hydrophilic polypeptides.

372


(Continued)


Hardware Description Size (mm) Particle Size (µm)300SB-C18USP L1

300SB-C8USP L7

300SB-CNUSP L10

300SB-C3USP L56

300-DiphenylUSP L11

Standard Columns (no special hardware required)Semi-Preparative 9.4 x 250 5 880995-202 880995-206 880995-205 880995-209Analytical 4.6 x 250 5 880995-902 880995-906 880995-905 880995-909Analytical 4.6 x 150 5 883995-902 883995-906 883995-905 883995-909Analytical 4.6 x 50 5 860950-902 860950-906 860950-905 860950-909Rapid Resolution 4.6 x 150 3.5 863973-902 863973-906 863973-905 863973-909Rapid Resolution 4.6 x 100 3.5 861973-902 861973-906Rapid Resolution 4.6 x 50 3.5 865973-902 865973-906 865973-905 865973-909Solvent Saver Plus 3.0 x 150 3.5 863974-302 863974-306 863974-309Solvent Saver Plus 3.0 x 100 3.5 861973-306Narrow Bore 2.1 x 250 5 881750-902Narrow Bore 2.1 x 150 5 883750-902 883750-906 883750-905 883750-909Narrow Bore RR 2.1 x 150 3.5 863750-906Narrow Bore RR 2.1 x 100 3.5 861775-902 861775-906Narrow Bore RR 2.1 x 50 3.5 865750-902 865750-906Narrow Bore RRHD 2.1 x 100 1.8 858750-902 858750-906 858750-909 858750-944Narrow Bore RRHD 2.1 x 50 1.8 857750-902 857750-906 857750-909 857750-944MicroBore 1.0 x 250 5 861630-902MicroBore RR 1.0 x 150 3.5 863630-902 863630-906MicroBore RR 1.0 x 50 3.5 865630-902 865630-906MicroBore Guard, 3/pk 1.0 x 17 5 5185-5920 5185-5920Guard Cartridge, 2/pk 9.4 x 15 7 820675-124 820675-124 820675-124 820675-124Guard Cartridge, 4/pk 4.6 x 12.5 5 820950-921 820950-918 820950-923 820950-924Guard Cartridge, 4/pk 2.1 x 12.5 5 821125-918 821125-918 821125-924 821125-924Guard Hardware Kit 840140-901 840140-901 840140-901 840140-901Guard Hardware Kit 820999-901 820999-901 820999-901 820999-901



PrepHT Cartridge Columns (require endfittings kit 820400-901)PrepHT Cartridge 21.2 x 250 7 897250-102 897250-106 897250-105 897250-109PrepHT Cartridge 21.2 x 150 7 897150-102 897150-106 897150-109PrepHT Cartridge 21.2 x 150 5 895150-902 895150-906 895150-909PrepHT Cartridge 21.2 x 100 5 895100-902 895100-906 895100-909PrepHT Cartridge 21.2 x 50 5 895050-902 895050-906 895050-909PrepHT Endfittings, 2/pk 820400-901 820400-901 820400-901 820400-901PrepHT Guard Cartridge,2/pk

17.0 x 7.5 5 820212-921 820212-918 820212-924 820212-924

Guard Cartridge Hardware 820444-901 820444-901 820444-901 820444-901

Capillary 0.5 x 250 5 5064-8266Capillary 0.5 x 150 5 5064-8264Capillary 0.5 x 35 5 5064-8294Capillary RR 0.5 x 150 3.5 5064-8268Capillary RR 0.5 x 35 3.5 5065-4459Capillary 0.3 x 250 5 5064-8265Capillary 0.3 x 150 5 5064-8263Capillary 0.3 x 35 5 5064-8295Capillary RR 0.3 x 150 3.5 5064-8267 5065-4460Capillary RR 0.3 x 100 3.5 5064-8259 5065-4461Capillary RR 0.3 x 35 3.5 5064-8270 5065-4462


Hardware Description Size (mm) Particle Size (µm)300SB-C18USP L1

300SB-C8USP L7

300SB-CNUSP L10

300SB-C3USP L56

300-DiphenylUSP L11

Capillary Glass-lined Columns

Capillary RR 0.3 x 50 3.5 5064-8300 5065-4463Nano Columns (PeeK fused silica)

Nano RR 0.1 x 150 3.5 5065-9910Nano RR 0.075 x 150 3.5 5065-9911Nano RR 0.075 x 50 3.5 5065-9924 5065-9923Trap/Guard, 5/pk 0.3 x 5 5 5065-9913 5065-9914Trap/Guard Hardware kit 5065-9915 5065-9915

374


ZorBAX rrHD 300-Diphenyl



SurfaceArea

TempLimits pH range endcapped

CarbonLoad

ZORBAX RRHD 300-Diphenyl 300Å 45 m2/g 80 °C 1.0-8.0 Yes 1.9%


Utilizing the same unique chemistry as the Pursuit 3.5 µm and 5 µm Diphenyl columns, the unique wide pore300Å Diphenyl phase offers additional selectivity through pi-pi interactions with aromatic amino acids in theprimary sequence. Agilent ZORBAX 1.8 µm 300Å Rapid Resolution High Definition (RRHD) columns bringUHPLC performance to the reversed-phase separation of intact proteins and protein digests.

The diphenyl column can be used for:

• Analysis of intact and modified proteins and polypeptides including protein structural analysis• Detection of post-translational modifications• Impurity analysis• Confirming protein identity

The ZORBAX RRHD 300-Diphenyl provides:

• Stability at low pH – allowing you to run your protein and peptide separations down to pH 1 usingtrifluoroacetic acid (TFA), and formic acid eluents with complete confidence

• Temperature stability – you can run your separations up to 80 °C to improve efficiency and reduceeluent viscosity, without compromising column lifetime

• UHPLC compatible – enabling higher order characterization with reduced analysis time

1 2 3 4 5

0

20

40

60

80

100

120

0.47

9

0.49

9 0

.594

0.95

3

4.11

9

4.29

9

1 2 3 4 5

0 20 40 60 80

100 120

0.45

4 0.50

1 0

.569

0.76

6

3.89

7 4

.010



Description Dimensions Particle Size (µm) Part No.ZORBAX RRHD 300-Diphenyl 2.1 x 50 1.8 857750-944ZORBAX RRHD 300-Diphenyl 2.1 x 100 1.8 858750-944

Light chain Heavy chain 1 Heavy chain 2

Light chain Heavy chain 1 Heavy chain 2

fast separation of reduced monoclonal antibodyColumn: Agilent ZorBAX rrHD 300-Diphenyl

858750-9442.1 x 100 mm, 1.8 µm

Mobile Phase: A: 0.1% TFA in waterB: 80% n-propyl alcohol,

10% ACN, 9.9% water, and 0.1% TFA

Sample: Reduced monoclonal antibody (IgG1) (1.0 mg/mL)

SampleInjection:

2 µL


Gradient: 0 min-1%B, 2 min-20% B, 5 min-50% B

Temperature: 74 °C

Detector: UV, 280

376


ZorBAX 300Å extend-C18• Rugged, high and low pH separations of polypeptides and peptides from pH 2-11.5• Different selectivity possible at high and low pH• High efficiency and good recovery of hydrophobic peptides at high pH• Ideal for LC/MS with ammonium-hydroxide-modified mobile phase

Agilent ZORBAX 300Å Extend-C18 is a wide-pore HPLC column for high efficiency separations of peptidesfrom pH 2-11.5. The unique, bidentate bonded phase provides excellent lifetime and reproducibility at highand low pH. At high pH, retention and selectivity of peptides and polypeptides can change dramatically as a result of changes in charge on molecules. Excellent recoveries of hydrophobic polypeptides have beenachieved at room temperature and high pH. LC/MS sensitivity of peptides and polypeptides can also beimproved at high pH using a simple ammonium-hydroxide-containing mobile phase.



SurfaceArea

Temp.Limits* pH range endcapped

CarbonLoad

ZORBAX 300Å Extend-C18 300Å 45 m2/g 60 °C 2.0-11.5 Double 4%

Specifications represent typical values only.*Temperature limits are 60 °C up to pH 8, 40 °C from pH 8-11.5.

Novel Bidentate C18-C18 Bonding for Extend-C18 Bonded Phase

TiPS & TooLS

Selecting the right column is onlypart of the total solution. Don't forgetkey supplies such as our wide rangeof LC lamps. Turn to page 90.


LC/MS analysis of angiotensin on extend-C18Column: ZorBAX extend-C18

773700-9022.1 x 150 mm, 5 µm

Mobile Phase: Acidic Conditions: A: 0.1% TFA in water B: 0.085% TFA in 80% acetonitrile (ACN)Basic Conditions: A: 10 mM NH4OH in water B: 10 mM NH4OH in 80% ACN



Temperature: 35 °C

MS Conditions: Pos. Ion ESI- Vf 70 V, Vcap 4.5 kV,N2- 35 psi, 12 L/min., 325 °C

Sample: 2.5 µL sample (50 pmol each)Angiotensin I, II, III

AAngiotensin IMax: 10889Low pH

BAngiotensin IMax: 367225High pH

LC30003

Time (min)

AII + AIII

AII

AIII

AI

13.2

61

12.0

50

5.49

9

8.47

7

9.62

1AI

TIC

(200

-150

0 m

/z)

2.500

5.0 7.5 10 12.5

1.0E6

2.0E6

3.0E6

4.0E6

5.0E6

m/z

227.

125

0.9

340.

339

8.0

433.

0

649.

565

9.7

720.

376

7.3 84

4.8

1025

.2

1179

.1

1277

.913

26.3

1373

.3

1468

.8

458.

0

+3 +2

433.

0

649.

065

9.8

+3

+2

1296

.6

+1

50000

1000

20

40

60

80

100

Time (min)

TIC

(200

-150

0 m

/z)

2.500

5.0 7.5 10 12.5

1.0E7

2.0E7

3.0E7

4.0E7

5.0E7

m/z50000

1000

20

40

60

80

100

Both small and large peptides demonstrate selectivity changes at high and low pH. At high pH, due to a change in charge, all three Angiotensins can be resolved. In addition, the spectral clarity of Angiotensin I is dramatically improved at high pH with the ammonium hydroxide mobile phase. The Extend-C18 column can be used for the analysis of small peptides at high pH as well.

Reference: B.E. Boyes. Separation and Analysis of Peptides at High pH Using RP-HPLC/ESI-MS, 4th WCBP, San Francisco, CA, Jan. 2000.


378


Long life at high pH with 300extend-C18Column: ZorBAX extend-C18

773450-9024.6 x 150 mm, 5 µm

Mobile Phase: 20% 20 mM NH4OH, pH 10.580% Methanol


Temperature: Aging 24 °CTests 40 °C

LC30001Column Volumes of Mobile Phase

k Va

lues

0 10,000 20,000 30,000 50,00040,0000

2

4

6

8

Each 10,000 column volume is approximately one working month.

4-Chloro-1-nitrobenzene

Trimipramine

Use ZorBAX extend-C18 for alternateselectivity at high pHColumn: ZorBAX extend-C18

773700-9022.1 x 150 mm, 5 µm

Mobile Phase: A: 0.1% TFA in WaterB: 0.085% TFA in 80% ACN

A: 20 mM NH4OH in WaterB: 20 mM NH4OH in 80% ACN



Temperature: 25 °C

MS Conditions: Pos. Ion ESI-Vf 70V, Vcap 4.5 kVN2 – 35 psi, 12 L/min, 300 °C4 µL (50 ng each peptide)

LCBP017Time (min)

LHG

A

B

LHL

LLLLLVF

LLL-NH2

LHG

LHL

LLL

LLVF

LLL-NH2

.5E7

1E7

1.5E7

2E7

2.5E7

3E7

42 8 10 12 14 16 18 200

0 6

.5E7

1E7

1.5E7

2E7

2.5E7

3E7

42 8 10 12 14 16 18 200

0 6

The Extend column can be used for high pH separations of peptides.At high and low pH, very different selectivity can result. Just bychanging pH, a complimentary method can be developed and it ispossible to determine if all peaks are resolved. The Extend columncan be used at high and low pH, so the complimentary separationcan be investigated with one column. Better MS sensitivity for thissample is also achieved at high pH.



ZorBAX 300Å extend-C18Hardware Description Size (mm) Particle Size (µm) Part No.

Analytical 4.6 x 250 5 770995-902Analytical 4.6 x 150 5 773995-902Rapid Resolution 4.6 x 150 3.5 763973-902Rapid Resolution 4.6 x 100 3.5 761973-902Rapid Resolution 4.6 x 50 3.5 765973-902Narrow Bore RR 2.1 x 150 3.5 763750-902Narrow Bore RR 2.1 x 100 3.5 761775-902Narrow Bore RR 2.1 x 50 3.5 765750-902Guard Cartridge, 4/pk 4.6 x 12.5 5 820950-932Guard Cartridge, 4/pk 2.1 x 12.5 5 821125-932Guard Hardware Kit 820999-901

Capillary Glass-lined ColumnsCapillary RR 0.3 x 150 3.5 5065-4464Capillary RR 0.3 x 100 3.5 5065-4465Capillary RR 0.3 x 75 3.5 5065-4466Capillary RR 0.3 x 50 3.5 5065-4467

380


Poroshell 300• UHPLC separations of biomolecules with superficially porous particles• 300Å pore provide high efficiency and recovery with proteins (up to 1,000 kDa)

and monoclonal antibodies• Achieve long lifetime at low pH with Poroshell 300SB; at high pH with 300Extend-C18• Optimize recovery and selectivity with four different bonded phases – 300SB-C18, 300SB-C8,

300SB-C3, and 300Extend-C18

Agilent Poroshell 300 columns are ideal for fast separations of proteins and peptides because thesuperficially porous particle allows for fast flow rates to be used while maintaining sharp, efficient peaks.Peptides and proteins are typically separated slowly to reduce the potential peak broadening of these slowdiffusing analytes. However, Poroshell columns use a superficially porous particle made with a thin layer ofporous silica, 0.25 µm thick, on a solid core of silica. This reduces the diffusion distance for proteins makingpractical rapid HPLC separations of peptides and proteins up to 500-1,000 kDA possible with 400/600 barHPLC systems, including the Agilent 1260 Infinity Bio-inert. Poroshell columns bonded with StableBondbonded phases provide excellent stability and selectivity choices with TFA and formic acid mobile phases.The Poroshell 300Extend-C18 column can be used from pH 2-11 for unique separations. These columns canbe used for analytical protein separations as well as LC/MS separations.

Solid core, 4.5 µm diameter

Porous shell, 0.25 µm thick


Bonded Phase Pore Size Temp. Limits* pH range endcappedPoroshell 300SB-C18, C8, C3 300Å 90 °C 1.0-8.0 NoPoroshell 300Extend-C18 300Å 40 °C above pH 8

60 °C below pH 8 2.0-11.0 Yes

Specifications represent typical values only.*300StableBond columns are designed for optimal use at low pH. At pH 6-8, highest column stability for all silica-basedcolumns is obtained by operating at temperatures <40 °C and using low buffer concentrations in the range of 0.01-0.02 M.At mid or high pH, 300Extend-C18 is recommended.

Poroshell 300 Columns



Poroshell 300 columns separate proteins and peptides in secondsColumn: Poroshell 300SB-C18

660750-9022.1 x 75 mm, 5 µm

Mobile Phase: A: 0.1% TFA in H20B: 0.07% TFA in ACN


Gradient: 5-100% B in 1.0 min

Temperature: 70 °C, 260 bar pressure

Detector: 215 nm

Sample: Proteins and Peptides

This separation of eight polypeptides and proteins is completed in less than 60 seconds. Each peak is sharp and efficient. LCPO001

Time (min)0.50 1.0

1

2

3

4

5

67

8

1. Angiotensin II2. Neurotensin3. RNase4. Insulin5. Lysozyme6. Myoglobin7. Carbonic Anhydrase8. Ovalbumin

Further information can be found in the following publications:

Poroshell 300SB-C18 (publication # 5988-2100ENUS)

Rapid HPLC Analysis of Monoclonal Antibody IgG1 Heavy Chains Using ZORBAX Poroshell 300SB-C8 (publication # 5989-0070EN)

Use of Temperature to Increase Resolution in the Ultrafast HPLC Separation of Proteins with ZORBAX Poroshell 300SB-C8 HPLC Columns(publication # 5989-0589EN)

Using the High-pH Stability of ZORBAX Poroshell 300Extend-C18 to Increase Signal-to-Noise in LC/MS (publication # 5989-0683EN)


TiPS & TooLS

382


reduce peptide map analysis time by 90% with Poroshell 300SBColumn A: Poroshell 300SB-C18

660750-9022.1 x 75 mm, 5 µm

Column B: ZorBAX 300SB-C18883750-9022.1 x 150 mm, 5 µm

Mobile Phase: A: 95% H2O, 5% ACN, 0.1% TFAB: 5% H2O, 95% ACN, 0.07% TFA

Flow Rate: 1 mL/min0.208 mL/min

Gradient: 0-100% B = 12 min0-100% B = 120 min

Temperature: 70 °C

Sample: 20 µL (0.22 µg/1 µL)BSA Tryptic Digest(15 hours, 70 pmol)

LCPO002

Time (min)

A

1 2 3 4 5 6 7 8

Time (min)

B

20 30 40 50 60 70 8010

A single chromatographic run of a protein tryptic digest can require one hour or more to complete. With Poroshell columns, the same complex separation can be completed in1/10th the time.

MicroBore Poroshell 300 columns provide maximum sensitivity for LC/MSColumn: Poroshell 300SB-C18

661750-9021.0 x 75 mm, 5 µm

Mobile Phase: A: Water + 0.1% Formic AcidB: ACN + 0.1% Formic Acid


Gradient: 20-100% B in 5.5 min

Temperature: 80 °C

MS Conditions: LC/MS: Pos. Ion ESI – Vcap 6000 VDrying Gas Flow: 12 L/minDrying Gas Temperature: 350 °CNebulizer: 45 psiFragmentor Volatage: 140 VScan: 600-2500Stepsize: 0.15 amuPeak width: 0.06 min

Sample: 1 µLLCPO003

Time (min)0.50 4.01.0 1.5 2.0 2.5 3.0 3.5

0.50.751.02.55.0

20000000

40000000

60000000

80000000

1EB

With narrow bore diameters of 2.1 mm, 1.0 mm, and 0.5 mm, Poroshell columns make an ideal LC/MS partner. When the sample is very limited, the 1.0 mm or 0.5 mm idPoroshell columns are an excellent choice for high sensitivity LC/MS analyses. Sensitive MS molecular weight determinations are possible with as little as 0.5 to 5 pmole ofprotein on Poroshell columns. Poroshell columns have also been used for rapid MS identification of intact proteins, even in the presence of stabilizers and tissue culture media.



Monoclonal igG1 chains: Separation on Poroshell 300SB-C8Column: Poroshell 300SB-C8

660750-9062.1 x 75 mm, 5 µm

Mobile Phase: A: 90% water: 10% ACN + 3 mL/L of MW 300 PEGB: 10% water: 90% ACN + 3 mL/L of MW 300 PEG


Gradient: 0 min 25% B10 min 40% B10.1 min 25% B12 min 25% B

Temperature: 70 °C

Sample: Monoclonal IgG1

min0 2 4 6 8 10

mAU

0

40

80

120

min0 2 4 6 8 10

mAU

0

40

80

120

minIgG_Poroshell

0 2 4 6 8 10

mAU

0

40

80

120

Courtesy of:Novartis Pharma,Biotechnology, BaselDr. Kurt ForrerPatrik Roethlisberger

Light ChainsHeavy Chains

Glycosylated? Non-Glycosylated?

igG treated with:DTT

igG treated with:DTTPeptide-N-Glycosidase F

igG treated with:DTTPeptide-N-Glycosidase FCarboxypeptidase-B

TiPS & TooLS

Agilent offers an extensive selection of certified chromatography sample vials including polypropylene and deactivated and siliconized glass. For more information see (publication # 5990-9022EN).


384


Protein elution pattern on ZorBAX Poroshell 300SB-C8Column: Poroshell 300SB-C8

660750-9062.1 x 75 mm, 5 µm

Mobile Phase: A: 0.1% TFA in H20B: 0.1% TFA in ACN


Gradient: B: 20 to 70% in 3 min

Detector: UV (214 nm)

500

453

406

359

312

265

218

171

124

77

300 21 42 63 84 105 126 147 168 189 210

0 21 42 63 84 105 126 147 168 189 210

0 21 42 63 84 105 126 147 168 189 210

Time (s)

1

234

56

7

8

490

444

398

352

306

260

214

168

122

76

30

Time(s)

Prot Elution

1

2 34

56 7

8

480

435

390

345

300

255

210

165

120

75

30

Time (s)

1

234

5 6

7

8

1. Glycoprotein X, MW ~ 22 kDa2. Protein I, MW ~ 4 kDa3. Glucagon, MW ~ 3.5 kDa4. Biosynthetic human insulin, MW ~ 6 kDa5. Protein J, MW ~ 3 kDa6. Protein K, MW ~ 6 kDa7. Glycoprotein Y, MW ~ 45 kDa8. Glycoprotein Z, MW ~ 30 kDa

Poroshell 300

Hardware DescriptionSize(mm)

Particle Size(µm)

Poroshell300SB-C18

Poroshell300SB-C8

Poroshell300SB-C3

Poroshell300extend-C18

Narrow Bore 2.1 x 75 5 660750-902 660750-906 660750-909 670750-902MicroBore 1.0 x 75 5 661750-902 661750-906 661750-909 671750-902Capillary 0.5 x 75 5 5065-4468Guard Cartridge, 4/pk 2.1 x 12.5 5 821075-920 821075-918 821075-924Guard Hardware Kit 820999-901 820999-901 820999-901MicroBore Guard, 3/pk 1.0 x 17 5 5185-5968 5185-5968 5185-5968 5185-5968

Column Temperature 40 °C



Resp

onse

(mV)

Resp

onse

(mV)

Resp

onse

(mV)



Poroshell 120• 120Å pore size for shorter chain peptide mapping• UHPLC performance on 600 bar systems• Up to 90% of the efficiency of sub-2 µm• 2X the efficiency of 3.5 µm• Up to 50% less pressure than sub-2 µm columns

Agilent Poroshell 120 columns are a 2.7 µm particle with a 1.7 µm solid core and 0.5 µm porous outer layer.This small particle size provides high efficiency, similar to sub-2 µm columns, but with 40-50% less pressure.These high efficiency, high resolution columns can be used on any type of LC. The porous outer layer andsolid core limit diffusion distance and improve separation speed while the narrow particle size distributionimproves efficiency and resolution. The columns can support high pressure and multiple columns can beused for the highest resolution and efficiency possible. The smaller 120Å pore size is ideal for fast highresolution analysis of small hydrophilic peptides in protein digests.


Bonded Phase Pore Size Temp Limits pH range endcappedCarbonLoad

EC-C18 120Å 60 °C 2.0-8.0 Double 10%SB-C18 120Å 90 °C 1.0-8.0 No 8%


For information on the full family of Poroshell 120 phases,see page 228.

386


Poroshell 120

Description Size (mm)Particle Size

(µm)eC-C18USP L1

SB-C18USP L1

Analytical 4.6 x 150 2.7 693975-902 683975-902Analytical 4.6 x 100 2.7 695975-902 685975-902Solvent Saver 3.0 x 150 2.7 693975-302 683975-302Solvent Saver 3.0 x 100 2.7 695975-302 685975-302Narrow Bore 2.1 x 150 2.7 693775-902 683775-902Narrow Bore 2.1 x 100 2.7 695775-902 685775-902



PLrP-S• Contain durable and resilient polymer particles that deliver reproducible results over longer lifetimes• Thermally and chemically stable• Comply with USP L21 designation• Used in bioscience, chemical, clinical research, energy, environmental, food and agriculture, material

science and pharmaceutical industries• Pore sizes (100Å-4000Å) for separations of small molecules to large complexes and polynucleotides

The PLRP-S family of columns consists of a range of pore sizes and particle sizes, all with identical chemistryand fundamental adsorptive characteristics. The particles are inherently hydrophobic, therefore no bondedphase, alkyl ligand is required for reversed-phase separations. This gives a highly reproducible material thatis free from silanols and heavy metal ions. Columns within the extensive product range are suitable fornano/capillary separations, including both bottom-up and top-down proteomics, analytical separations, and preparative purifications. In addition, process columns can be packed with bulk media.



3 µm: 4000 psi (300 bar)

PLrP-S Applications

Pore Size Application100Å Small molecules/peptides/oligonucleotides300Å Recombinant peptides/proteins1000Å Large proteins4000Å DNA/high speed

Scanning electron micrographs (SeM) of PLrP-S 10 µm particles.The difference in pore size is clearly seen.A is the small pore 100ÅB the larger pore 300ÅC the gigaporous 4000Å

BA C

10 µm 10 µm 10 µm

388


HPLC of 25 bp DNA ladder Column: PLrP-S, 2.1 x 150 mmMobile Phase: A: 0.1 M TEAA

B: 0.1 M TEAA in 50% water:50% ACN


Gradient: 12.5-50% B in 150 min

HPLC

PLRP-S 100Å

PLRP-S 300Å

PLRP-S 1000Å

PLRP-S 4000Å

Resp

onse

, UV,

260

nm

TimeVLCPLRPSResp

Polyethylene glycolsColumn: PLrP-S 100Å

PL1111-35004.6 x 150 mm, 5 µm

Mobile Phase: A: WaterB: ACN

Gradient: 10-30% B in 12 min, held at 30% B for 3 min



Sample Conc: 1 mg/mL

Detector: ELS (neb=50 °C, evap=70 °C, gas=1.6 SLM)0

PEG 400

PEG 1080

VLC0048

15

0 15

min

min



exploiting chemical stability – TfA concentrationColumn: PLrP-S 100Å

PL1512-55004.6 x 250 mm, 5 µm

Mobile Phase: A: TFA (various %) in waterB: TFA (various %) in ACN




321

0.1%

0.02%

0.0025%

min0 15

VLC0068

1. Angiotensin III2. Angiotensin II3. Angiotensin I

Selectivity in peptide rP-LCColumn: PLrP-S 100Å

PL1512-55004.6 x 250 mm, 5 µm

Mobile Phase: A: 0.1% TFA/1% 2-Propanol/WaterB: 0.1% TFA/1% 2-Propanol/ACN


Gradient: 95% A (0-3 min) to 50% A (13 min)


Good separation of peptide standards on Agilent PLRP-S

1. YG2. GYG3. PY4. YV5. YY6. GLY7. YF8. GFL9. YGGFM

10. Oxalic acid (marker)11. Benzoic acid (marker)

(see J.Chromatography 512 (1990) 315-23)

390


exploiting chemical stability – NH4oH concentrationColumn: PLrP-S 100Å

PL1512-55004.6 x 250 mm, 5 µm

Mobile Phase: A: NH4OH (various mM) in waterB: NH4OH (various mM) in ACN




0

1 mM

10 mM

100 mM

VLC0049

10 min

1

2

3

1. Angiotensin II2. Angiotensin I3. Angiotensin III

Alberta Peptide institute test mixColumn: PLrP-S 100Å

PL1512-55004.6 x 250 mm, 5 µm





0

4

5

VLC0050

30min

12

3

1. Ala3-Gly4 (free amino)2. Gly3-Gly4 (Na-acetylated)3. Ala3-Gly4 (Na-acetylated)4. Val3-Gly4 (Na-acetylated)5. Val3-Val4 (Na-acetylated)



0

0

25

min

mV

12.5

0

0

25

min

mV

12.5

0

0

25 12

1 2

1 2

80 ºC

60 ºC

35 ºC

min

mV

12.5

VLC0072

Temperature as a tool to enhance mass transferand improve resolution of oligonucleotides in ion-pair reversed-phase HPLCColumn: PLrP-S 100Å

PL1512-13004.6 x 50 mm, 3 µm

Mobile Phase: A: 100 mM TEAAB: 100 mM TEAA in 25% ACN

Gradient: 5% change in buffer B over 5 min


Temperature: 35 °C, 60 °C, or 80 °C


1. 29-mer2. 30-mer

2

31

min0 24 VLC0074

1. a-Lactalbumin2. b-Lactoglobulin (B chain)3. b-Lactoglobulin (A chain)

whey proteins in dairy samples – milkColumn: PLrP-S 300Å

PL1512-38014.6 x 150 mm, 8 µm


Gradient: 36-48% B, 0-24 min, 48-100% B, 24-30 min100% B, 30-35 min, 100-36% B, 35-40 min




392


0 12VLC0051

min 0 18min

1

PLRP-S 300Å PLRP-S 1000Å

2

1

2

1. Collagen (120,000 MW)2. Fibrinogen (340,000 MW)

Large fibrous proteinsColumn: PLrP-S 300Å

PL1512-38014.6 x 150 mm, 8 µm

Column: PLrP-S 1000ÅPL1512-38024.6 x 150 mm, 8 µm

Mobile Phase: A: 0.25% TFA in waterB: 0.25% TFA in 5% water:95% ACN






PLrP-S HPLC Columns

Hardware Size (mm)Particle Size

(µm)

PLrP-S100ÅUSP L21

PLrP-S300ÅUSP L21

PLrP-S1000ÅUSP L21

PLrP-S4000ÅUSP L21

4.6 x 250 8 PL1512-5800 PL1512-5801 PL1512-58024.6 x 150 8 PL1512-3800 PL1512-3801 PL1512-3802 PL1512-38034.6 x 50 8 PL1512-1801 PL1512-1802 PL1512-18034.6 x 250 5 PL1512-5500 PL1512-55014.6 x 150 5 PL1111-3500 PL1512-35014.6 x 50 5 PL1512-1500 PL1512-1501 PL1512-1502 PL1512-15034.6 x 150 3 PL1512-3300 PL1512-33014.6 x 50 3 PL1512-1300 PL1512-13012.1 x 250 8 PL1912-58012.1 x 150 8 PL1912-3801 PL1912-3802 PL1912-38032.1 x 50 8 PL1912-1801 PL1912-1802 PL1912-18032.1 x 250 5 PL1912-5500 PL1912-55012.1 x 150 5 PL1912-3500 PL1912-35012.1 x 50 5 PL1912-1500 PL1912-1501 PL1912-1502 PL1912-15032.1 x 150 3 PL1912-3300 PL1912-33012.1 x 50 3 PL1912-1300 PL1912-13011.0 x 50 8 PL1312-18021.0 x 50 5 PL1312-1500 PL1312-15021.0 x 10 5 PL1C12-25021.0 x 150 3 PL1312-33001.0 x 50 3 PL1312-1300PLRP-S Guard Cartridges for 5 x 3 mm, 2/pk

PL1612-1801 PL1612-1801 PL1612-1801 PL1612-1801

Guard Cartridge holder for 3.0 x 5.0 mm cartridges

PL1310-0016 PL1310-0016 PL1310-0016 PL1310-0016

TiPS & TooLS

For prep columns and mediaordering information,

For microbore columns ordering information,turn to page 463.

turn to pages 470-471.

394


Amino Acid Analysis (AAA) Columns and Supplies

• High resolution and rapid analysis of 24 amino acids• Tested for amino acid analysis• Uses well-known OPA and FMOC precolumn derivatization chemistry• Easily automated using a detailed online, derivatization protocol available for use with Agilent

1100/1200 autosampler

The Agilent ZORBAX Eclipse AAA high efficiency column rapidly separates amino acids following anupdated and improved protocol. Total analysis from injection-to-injection can be achieved in as little as 8 min (7 min analysis time) on a 50 mm 1.8 µm column, 14 min (9 min analysis time) on shorter, 75 mmlength columns and 24 min (18 min analysis time) on the 150 mm column length. Exceptional sensitivity (5-50 pmol with DAD, FLD) and reliability are achieved using both OPA and FMOC derivatizationchemistries in one fully automated procedure using the Agilent 1100/1200 HPLC instrument.

ZorBAX eclipse Amino Acid Analysis (AAA) Columns

TiPS & TooLS

Further information can be found in thefollowing publication:

High-Speed Amino Acid Analysis (AAA)on 1.8 µm Reversed-Phase (RP) Columns(publication # 5989-6297EN)


ZorBAX eclipse Amino Acid Analysis (AAA) ColumnsHardware Description Size (mm) Particle Size (µm) Part No.

Analytical routine sensitivity 4.6 x 150 5 993400-902Analytical routine sensitivity, high-resolution using FLD

4.6 x 150 3.5 963400-902

Analytical routine sensitivity, high-throughput

4.6 x 75 3.5 966400-902

Solvent Saver high sensitivity, high-resolution

3.0 x 150 3.5 961400-302

Guard Cartridges, 4/pk 4.6 x 12.5 5 820950-931Guard Hardware Kit 820999-901

ZORBAX Eclipse Plus C18 columns are another excellentchoice for Amino Acid Analysis. For more information aboutZORBAX Eclipse Plus Columns, see page 248.



Amino Acid StandardsEach amino acid standard contains the following amino acids:

• Glycine• L-cysteine• L-histidine• L-tyrosine• L-leucine• L-methionine

• L-serine• L-alanine• L-phenylalanine• L-glutamic acid• L-proline• L-isoleucine

• L-arginine• L-threonine• L-valine• L-lysine• L-aspartic acid

Amino Acid Standards, 10 x 1 mL ampoules*Description Part No.1 nmol/µL 5061-3330250 pmol/µL 5061-3331100 pmol/µL 5061-333225 pmol/µL 5061-333310 pmol/µL 5061-3334Amino acids supplement kitIncludes 1 g each of norvaline, sarcosine, asparagine, glutamine, tryptophan, and 4-hydroxyproline

5062-2478

*Consider shelf-life and buy limited quantities, P/N 5062-2478 ships as 1 g vials

Amino Acid Separations reagentsDescription Part No.OPA reagent, 10 mg/mL each in 0.4 M borate buffer o-phthalaldehyde (OPA) and 3-mercaptopropionic acid, 6 x 1 mL ampoules

5061-3335

FMOC reagent, 2.5 mg/mL in acetonitrile, 9-fluorenylmethylchloroformate, 1 mL, 10 ampoules 5061-3337Borate buffer, 100 mL 5061-3339DTDPA (Dithiodiproprionic) reagent, for analysis of cysteine, 5 g 5062-2479

396


High resolution of 24 amino acids using ZorBAX eclipse-AAA protocolColumn: ZorBAX eclipse AAA

963400-9024.6 x 150 mm, 3.5 µm

Mobile Phase: A: 40 mM Na2HPO4, pH 7.8B: ACN:MeOH:Water,45:45:10 v/v

Flow Rate: 2 mL/min

Temperature: 40 °C

Detector: Fluorescence

Sample: 24 Amino Acids

13. Cys14. Val15. Met16. Nva17. Trp18. Phe19. Ile20. Leu21. Lys22. Hyp23. Sar24. Pro

This high resolution separation of 24 amino acids is done in 18 minutes. If the Rapid Resolution 4.6 x 75 mm Eclipse AAA column is selected, these amino acids are resolved in 9 minutes.

LCPAH01

Time (min)

1

2

3

4

5

6

7

8

9

1011 12

14

15

16 1718

19

20

21

22 23

24

20 2510 150 5

1. Asp2. Glu3. Asn4. Ser5. Gln6. His7. Gly8. Thr9. Cit

10. Arg11. Ala12. Tyr



ion-exchange ChromatographyPurify proteins and other charged moleculesIon-exchange chromatography (IEX) is a highly sensitive technique that allows you to separate ions andpolar molecules based on their charge. Like SEC, IEX can be used to separate proteins in their native state.

Applying IEX to charge variant analysisDuring production and purification, antibodies can exhibit changes in charge heterogeneity as a result of amino acid substitutions, glycosylation, phosphorylation, and other post-translational or chemicalmodifications. Because these changes can impact stability and activity – or cause immunologically adversereactions – the analysis of charge heterogeneity in monoclonal antibody (MAb) preparations is critical tobiopharmaceuticals.

In protein analysis, charge variations at a given pH indicate a change in the primary molecular structure –resulting in additional forms of the protein in question. These are called isoforms (or charge variants), and can be resolved by IEX chromatography. IEX is also useful as a preparative technique.

The pages that follow describe Agilent’s family of weak and strong ion-exchangers – both anionic and cationic.

• Agilent non-porous Bio ieX columns are designed for high-resolution, high-efficiency, and high-recovery separations.

• Agilent Bio MAb columns are optimized for separating charge isoforms of monoclonal antibodies.• Agilent porous ieX columns (PL-SAX and PL-SCX) are chemically stable, and are available

in two pore sizes – allowing you to separate peptides, oligonucleotides, and very large proteins.• Bio-Monolith ieX columns are uniquely suited to separating antibodies, viruses, and DNA.

398


ion-exchange Column Selection

Application Agilent Columns NotesMonoclonal antibodies Agilent Bio MAb Thorough characterization of monoclonal antibodies includes the identification and

monitoring of acidic and basic isoforms. Agilent Bio MAb HPLC columns feature a uniqueresin specifically designed for high-resolution charge-based separations of monoclonalantibodies.

Peptides and proteins Agilent Bio IEX Agilent Bio Ion-Exchange columns are packed with polymeric, nonporous, ion-exchangeparticles. Bio IEX columns are designed for high resolution, high recovery and highlyefficient separations.

Proteins, peptides and deprotectedsynthetic oligonucleotides

PL-SAX The strong anion-exchange functionality, covalently linked to a fully porous chemicallystable polymer, extends the operating pH range. In addition, the anion-exchange capacityis independent of pH. For synthetic oligonucleotides, separations using denaturingconditions of temperature, organic solvent, and high pH are all possible. The 5 µm mediadelivers separations at high resolution with the 30 µm media used for medium pressureliquid chromatography.

ü 1000Åü 4000Å

Globular proteins and peptides PL-SAX 1000ÅVery large biomolecules/high speed PL-SAX 4000ÅSmall peptides to large proteins PL-SCX PL-SCX is a macroporous PS/DVB matrix with a very hydrophilic coating and strong

cation-exchange functionality. This process is controlled to provide the optimum density of strong cation-exchange moieties for the analysis, separation and purification of a widerange of biomolecules. The 5 µm media delivers separations at higher resolution with the30 µm media used for medium pressure liquid chromatography.

ü 1000Åü 4000Å

Globular proteins PL-SCX 1000ÅVery large biomolecules/high speed PL-SCX 4000ÅAntibodies (IgG, IgM), plasmid DNA,viruses, phages and other macrobiomolecules

Bio-Monolith Strong cation-exchange, strong and weak anion-exchange, and Protein A phases. Bio-Monolith HPLC columns are compatible with preparative LC systems, including Agilent 1100 and 1200 HPLC systems.ü Bio-Monolith QA

ü Bio-Monolith DEAEü Bio-Monolith SO3ü Bio-Monolith Protein A

Viruses, DNA, large proteins Bio-Monolith QAPlasmid DNS, bacteriophages Bio-Monolith DEAEProteins, antibodies Bio-Monolith SO3



Agilent Bio MAb HPLC Columns• A packing support composed of a rigid, spherical, highly cross-linked polystyrene divinylbenzene

(PS/DVB) non-porous bead• Particles grafted with a hydrophilic, polymeric layer, virtually eliminating non-specific binding of

antibody proteins• A different process is used to layer the weak cation-exchange phase to the particle making it a

higher density than the Agilent Bio WCX column particles• Specifically designed for the separation of charge isoforms of monoclonal antibodies

Thorough characterization of monoclonal antibodies includes the identification and monitoring of acidic and basic isoforms. Agilent Bio MAb HPLC columns feature a unique resin specifically designed for high-resolution, charge-based separations of monoclonal antibodies. Compatible with aqueous solution buffers, acetonitrile/acetone/methanol and water mixtures. Commonly used buffers: phosphate,tris, MES and acetate.

Bio MAb columns are available in 1.7, 3, 5 and 10 µm sizes, providing higher resolution with smaller particles.


Bonded Phase iDParticle

SizepH

Stability

operatingTemperature

Limit flow rateWeak Cation-Exchange(carboxylate)

2.1 and 4.6 mm 1.7, 3, 5and 10 µm

2-12 80 °C 0.1-1.0 mL/minTiPS & TooLS

Capillary electrophoresis is an alternative technique to liquidchromatography for the separation of charged isoforms. Further information can be found in the following Technical Note:

Capillary electrophoreseis focusing on the Agilent Capillary Electrophoresissystem (publication # 5989-9852EN)


400


2

0

20

40

60

80

100

120

mAU

4 6 8 10 12 14 16 18 min

2

020

40

60

80100

120140

mAU

4 6 8 10 12 14 16 18 minVLC_IE_Mab

Consistent ion-exchange MAb separationColumn: Bio MAb, PeeK

5190-24112.1 x 250 mm, 5 µm

Buffer: A: Sodium phosphate buffer, 20 mMB: Buffer A + 400 mM NaCl

Gradient: 15-35% Buffer B from 0-30 min


Sample: CHO-humanized MAb, 1 mg/mL

Injection: 2.5 µL

Detector: UV 220 nm


To provide a metal free flow path, Bio MAb PEEK columnsare available.

1st run

10th run

Virtually eliminate retention time variationsColumn: Bio MAb, stainless steel

5190-24134.6 x 250 mm, 10 µm

Mobile Phase: A: 10 mM phosphate, pH 6.0B: A + 1.0 M NaCl



Temperature: 25 °C

Detector: UV 214 nm

0 2

1 2 3

Lot A

Lot B

Lot C

4 6 8 10 12 14 min16 18

The combination of well-controlled resin production, column surface chemistry, and column packing virtually eliminates retention time variationsfrom column-to-column and lot-to-lot.

1. Cytochrome c2. Lysozyme3. Ribonuclease A



Charge isoform analysis of monoclonal antibodiesColumn: Bio MAb, PeeK

5190-24074.6 x 250 mm, 5 µm

Mobile Phase: A: 10 mM Sodium Phosphate, pH 7.50B: A + 100 mM NaCl, pH 7.50



Sample: 5 µL, 5 mg/mL, MAb

6420 8 10 12 14 16 18 20 22 24 26 28 30 32 34

0.00

0.30

0.20

0.40

0.50

0.60

0.10

High resolution separation of acidic and basic charge variants using the Agilent Bio MAb NP5 column

Absorbance (AU)

Time (min)

Acidic isoforms

Basic isoforms

Agilent Bio MAb HPLC Columns

Size (mm) Particle Size (µm)Bio MAbPeeK Pressure Limit

Bio MAbStainless Steel Pressure Limit

4.6 x 250 10 5190-2415 275 bar, 4000 psi 5190-2413 275 bar, 4000 psi4.6 x 50, Guard 10 5190-2416 275 bar, 4000 psi4.6 x 250 5 5190-2407 400 bar, 5800 psi 5190-2405 413 bar, 6000 psi4.6 x 50, Guard 5 5190-2408 400 bar, 5800 psi4.6 x 50 3 5190-2403 551 bar, 8000 psi4.6 x 50 1.7 5190-2401 600 bar, 8700 psi4.0 x 10, Guard 10 5190-2414 275 bar, 4000 psi4.0 x 10, Guard 5 5190-2406 413 bar, 6000 psi4.0 x 10, Guard 3 5190-2404 551 bar, 8000 psi4.0 x 10, Guard 1.7 5190-2402 600 bar, 8700 psi2.1 x 250 10 5190-2419 275 bar, 4000 psi2.1 x 50, Guard 10 5190-2420 275 bar, 4000 psi2.1 x 250 5 5190-2411 400 bar, 5800 psi2.1 x 50, Guard 5 5190-2412 400 bar, 5800 psi

402


Agilent Bio ieX HPLC Columns• Highly cross-linked and rigid nonporous poly(styrene divinylbenzene) (PS/DVB) particles

are grafted with a hydrophilic, polymeric layer, eliminating nonspecific binding• Uniform, densely packed ion-exchange functional groups are chemically bonded to the hydrophilic

layer (multiple ion-exchange groups per anchoring) to increase column capacity• Particles, coating and bonding are resistant to high pressures, promoting higher resolution

and faster separations• Multiple ion-exchange groups are captured on one anchoring to increase capacity

Agilent Bio IEX HPLC columns are packed with polymeric, nonporous, ion-exchange particles and are designed for high resolution, high recovery and highly efficient separations of peptides,oligonucleotides and proteins.

The Bio IEX family offers strong cation-exchange (SCX), weak cation-exchange (WCX), strong anion-exchange (SAX) and weak anion-exchange (WAX) phases. All phases are available in 1.7, 3, 5 and 10 µm non-porous particles sizes.

TiPS & TooLS

More information is a click away. We have a variety of educational primers, application notes, maintenance guides, and literature available from Agilent for free.

To learn more, visit www.agilent.com/chem/library


Bonded Phase iD Particle Size pH Stabilityoperating

Temperature Limit flow rate

SCX (Strong cation-exchange) - S03H 2.1 and 4.6 mm 1.7, 3, 5 and 10 µm 2-12 80 °C 0.1-1.0 mL/minWCX (Weak cation-exchange) - C00HSAX (Strong anion-exchange) - N(CH3)3WAX (Weak cation-exchange) - N(C2H5)2



0 2 4 6 8 10 12 min

mAU

10

20

30

40

1 2

3

4

5

exceptional separating powerColumn: Agilent Bio SCX, stainless steel

5190-24234.6 x 50 mm, 3 µm

Buffer: 10 mM Phosphate, pH 6.0


Gradient: 0-1.0 M NaCl, 15 min

Detector: 280 nm

1. Ovalbumin, 4.6 pl2. Ribonuclease A, 8.7 pl3. Cytochrome c, 9.6 pl4. Aprotinin, 10.0 pl5. Lysozyme, 11.0 pl

N > 100,000/50 mm for Lysozyme

The hydrophilic, polymeric layer and densely packed ion-exchange functionalgroups provide extremely sharp peak shapes and high resolution of a mixtureof proteins with a broad range of isoelectric points (pI).

Separation of protein standards on Agilent 3 µmion-exchange columns by cation-exchangechromatographyColumn A: Agilent Bio SCX, NP 3, 4.6 x 50 mm, SSColumn B: Agilent Bio wCX, NP 3, 4.6 x 50 mm, SSColumn C: Agilent Bio MAb, NP 3, 4.6 x 50 mm, SSMobile Phase: A: 10 mM NaH2PO4.2H2O, pH 5.70

B: A + 1 M NaCl


Gradient: 0 min - 100% A : 0% B25 min - 0% A : 100% B


Detector: Agilent 1260 Infinity Bio-inert Quaternary LC with diode array detector at 220 nm

Sample: Cytochrome c, ribonuclease A, lysozyme and protein mix

illustration that Bio wCX, SCX and MAb columns are capable of producing protein separations

Agilent column Peak number Peak name rT [min] Height [mAU] Area [mAU*s] Plates width [min] resolutionBio WCX NP, 3 µm 1 Cytochrome c 7.86 124 1833 7844 0.2089 -

2 RNase A 9.03 241 3358 10800 0.2044 3.323 Lysozyme 13.13 636 7274 44488 0.1466 13.73

Bio SCX NP, 3 µm 1 RNase A 7.06 396 2616 39847 0.0832 -2 Cytochrome c 7.66 297 2778 28920 0.1060 1.083 Lysozyme 10.49 763 7186 44828 0.1167 1.37

Bio MAb NP, 3 µm 1 Cytochrome c 10.04 203 2369 21814 0.1600 -2 RNase A 11.37 256 2690 33314 0.1467 3.113 Lysozyme 12.59 652 6616 56734 0.1244 5.28

12

3

1 2

3

1 2

3SCX

wCX

MAb

404


weak cation-exchange chromatography for P128 therapeutic protein sample on the Agilent 1260 Bio-inert Quaternary LC system using different cation-exchange columns

min22 23 24 25 26 27 28 29 30 31

mAU

050

100150200250300350400

24.

786

26.

359 26.

618

27.

564

mAU

0

50

100

150

200

250

300

350

25.

860

26.

867

mAU

20

40

60

80

100

120

140

23.

976

25.

210

min22 23 24 25 26 27 28 29 30 31

min22 23 24 25 26 27 28 29 30 31

Column A: Bio MAb, PeeK5190-24074.6 x 250 mm, 5 µm

Column B: Bio MAb, PeeK5190-24154.6 x 250 mm, 10 µm

Column C: Brand B wCX-104.0 x 250 mm, 10 µm

Mobile Phase: A: 20 mM sodium phosphate (pH = 6.0)B:20 mM sodium phosphate (pH = 6.0)

containing 1.0 M sodium chloride


Gradient: 10% B 0 min, 35% B 35 min, 10% B 36 min, 10% B 45 min

Detector: UV, 220 nm/4 nm, Reference: Off(data also acquired at 220, 230, 240, and 280 nm)

Sample: P128

Sample was desalted by ultrafiltration and extracted into 20 mMsodium phosphate.

A

B

C



Agilent Bio ieX HPLC Columns, PeeK

Size (mm) Particle Size (µm) Pressure LimitBio SCXPart No.

Bio wCXPart No.

Bio SAXPart No.

Bio wAXPart No.

4.6 x 250 10 275 bar, 4000 psi 5190-2435 5190-2455 5190-2475 5190-24954.6 x 50, Guard 10 275 bar, 4000 psi 5190-2436 5190-2456 5190-2476 5190-24964.6 x 250 5 400 bar, 5800 psi 5190-2427 5190-2447 5190-2467 5190-24874.6 x 50, Guard 5 400 bar, 5800 psi 5190-2428 5190-2448 5190-2468 5190-24882.1 x 250 10 275 bar, 4000 psi 5190-2439 5190-2459 5190-2479 5190-24992.1 x 50, Guard 10 275 bar, 4000 psi 5190-2440 5190-2460 5190-2480 5190-25002.1 x 250 5 400 bar, 5800 psi 5190-2431 5190-2451 5190-2471 5190-24912.1 x 50, Guard 5 400 bar, 5800 psi 5190-2432 5190-2452 5190-2472 5190-2492

Agilent Bio ieX HPLC Columns, Stainless Steel

Size (mm) Particle Size (µm) Pressure LimitBio SCXPart No.

Bio wCXPart No.

Bio SAXPart No.

Bio wAXPart No.

4.6 x 250 10 275 bar, 4000 psi 5190-2433 5190-2453 5190-2473 5190-24934.6 x 250 5 413 bar, 6000 psi 5190-2425 5190-2445 5190-2465 5190-24854.6 x 50 3 551 bar, 8000 psi 5190-2423 5190-2443 5190-2463 5190-24834.6 x 50 1.7 600 bar, 8700 psi 5190-2421 5190-2441 5190-2461 5190-24814.0 x 10, Guard 10 275 bar, 4000 psi 5190-2434 5190-2454 5190-2474 5190-24944.0 x 10, Guard 5 413 bar, 6000 psi 5190-2426 5190-2446 5190-2466 5190-24864.0 x 10, Guard 3 551 bar, 8000 psi 5190-2424 5190-2444 5190-2464 5190-24844.0 x 10, Guard 1.7 275 bar, 4000 psi 5190-2422 5190-2442 5190-2462 5190-2482

406


PL-SAX Strong Anion-exchange Columns• Small particles deliver excellent chromatographic performance• Wide range of particle sizes and 2 pore sizes for flexible analysis to scale-up purification• Exceptional stability for long column lifetime

PL-SAX -N(CH3)3+ is ideal for the anion-exchange HPLC separations of proteins, peptides and deprotected

synthetic oligonucleotides under denaturing conditions. The strong anion-exchange functionality, covalentlylinked to a chemically stable fully porous polymer, extends the operating pH range. In addition, the anion-exchange capacity is independent of pH. For synthetic oligonucleotides, separations using denaturing conditions of temperature, organic solvent, and high pH are all possible. PL-SAX deliversimproved chromatography for self-complementary or G-rich sequences that may associate to formaggregates or hairpin structures. The 5 µm material provides high efficiency separations of n and n-1 sequences. A wide range of particle sizes and column geometries permits analysis scale-up to purification. The strong anion-exchange functionality provides a material with exceptional chemical and thermal stability, even with sodium hydroxide eluents, leading to long column lifetime.


Bonded PhaseiD

(mm)Particle Size

(µm) Pore Size pH Stability

operatingTemperature

LimitStrong Anion-Exchange 2.1, 4.6, 7.5,

25, 50 and 100

5, 8, 10 and 30

1000Å and 4000Å

1-14 80 °C



Standard ion-exchange protein separationColumn: PL-SAX 1000Å

PL1551-15024.6 x 50 mm, 5 µm

Mobile Phase: A: 10 mM Tris HCl pH 8B: A+0.35 M NaCl pH 8




1. Myoglobin2. Bovine carbonic anhydrase3. Ovalbumin4. Soybean trypsin inhibitor

3

421

min0 25VLC0070

Analysis of choline kinase on PL-SAX 4000ÅColumn: PL-SAX

PL1551-18034.6 x 50 mm, 8 µm

Mobile Phase: A: 20 mM Tris 5% ethyleneglycol, pH 7.5(The following are requiredto retain enzyme activity)1.0 mM Ethylene glycoltetraacetic acid2.0 mM ß-Mercaptoethanol0.2 mMPhenylmethylsulfonyl fluorideB: A + 1 M KCI


Detector: UV, 280 nm0 min 40

0

%B100

Separation courtesy of T Porter, Purdue University, USA

enzyme activity

408


Analysis of representative whey proteinsColumn: PL-SAX 1000Å

PL1551-18024.6 x 50 mm, 8 µm

Mobile Phase: A: 0.02 M Tris HCI, pH 7B: A + 0.5 M CH3COONa, pH 7




0

1

2

3

4

min 18

1. Carbonic anhydrase2. a-lactalbumin3. b-lactoglobulin B4. b-lactoglobulin A

High resolution separation of a Poly-T-oligonucleotide size standard spiked with 10-mer, 15-mer, 30-mer and 50-mer (main peaks)Column: PL-SAX 1000Å

PL1551-18024.6 x 50 mm, 8 µm

Mobile Phase: A: 7:93 v/v ACN: 0.1 M TEAA, pH 8.5B: 7:93 v/v ACN: 0.1 M TEAA, 1 M ammonium chloride, pH 8.5

Gradient: 0-40% B in 10 min, followed by 40-70% B in 14 min and 70-100% B in 25 min


Temperature: 60 °C


0

0

200015

30 50

10

VLC0045

min 50



PL-SAX Strong Anion-exchange Columns

Size (mm) Particle Size (µm) Pressure LimitPL-SAX1000Å

PL-SAX4000Å

1.0 x 50 5 207 bar, 3000 psi PL1351-1502 PL1351-15032.1 x 50 5 207 bar, 3000 psi PL1951-1502 PL1951-15034.6 x 50 5 207 bar, 3000 psi PL1551-1502 PL1551-15032.1 x 50 8 207 bar, 3000 psi PL1951-1802 PL1951-18032.1 x 150 8 207 bar, 3000 psi PL1951-3802 PL1951-38034.6 x 50 8 207 bar, 3000 psi PL1551-1802 PL1551-18034.6 x 150 8 207 bar, 3000 psi PL1551-3802 PL1551-38034.6 x 250 10 207 bar, 3000 psi PL1551-5102 PL1551-51034.6 x 150 10 207 bar, 3000 psi PL1551-3102 PL1551-310325 x 50 10 207 bar, 3000 psi PL1251-1102 PL1251-110325 x 150 10 207 bar, 3000 psi PL1251-3102 PL1251-310350 x 150 10 207 bar, 3000 psi PL1751-3102 PL1751-3103100 x 300 10 207 bar, 3000 psi PL1851-2102 PL1851-21034.6 x 250 30 207 bar, 3000 psi PL1551-5702 PL1551-57034.6 x 150 30 207 bar, 3000 psi PL1551-3702 PL1551-370325 x 150 30 207 bar, 3000 psi PL1251-3702 PL1251-370350 x 150 30 207 bar, 3000 psi PL1751-3702 PL1751-3703100 x 300 30 207 bar, 3000 psi PL1851-3102 PL1851-3103

PL-SAX Strong Anion-exchange Bulk Media

Size Particle Size (µm)PL-SAX1000Å

PL-SAX4000Å

100 g 10 PL1451-4102 PL1451-41031 kg 10 PL1451-6102 PL1451-6103100 g 30 PL1451-4702 PL1451-47031 kg 30 PL1451-6702 PL1451-6703

410

COLUMNS FOR BIOMOLECULE SEPARATIONS

PL-SCX Strong Cation-Exchange Columns• Optimal design for effective separation of biomolecules• Pore sizes allow use of a range of solute sizes• Exceptional stability for long column lifetime

PL-SCX -SO3- is a macroporous PS/DVB matrix with a very hydrophilic coating and strong cation-exchange

functionality. This process is controlled to provide the optimum density of strong cation-exchange moietiesfor the analysis, separation and purification of a wide range of biomolecules, from small peptides to largeproteins. Two pore sizes are available, 1000Å and 4000Å, to provide good mass transfer characteristics fora range of solute sizes. The 5 µm media delivers separations at higher resolution with the 30 µm media usedfor medium pressure liquid chromatography.


Bonded PhaseID

(mm)Particle Size

(µm) Pore Size pH Stability

OperatingTemperature

LimitStrong Cation-Exchange 2.1, 4.6,

7.5, 25, 50and 100

5, 8, 10 and 30

1000Å and 4000Å

1-14 80 °C

0 2

1 2 3

Lot A

Lot B

Lot C

4 6 8 10 12 14 min16 18

1. Myoglobin2. Chymotrypsinogen A3. Cytochrome c4. Lysozyme

Standard protein separationColumn: PL-SCX 1000Å

PL1545-15024.6 x 50 mm, 5 µm

Mobile Phase: A: 20 mM KH2PO4, pH 6.0B: A + 1 M NaCl




411WWW.AGILENT.COM/CHEM/LC


PL-SCX Strong Cation-Exchange Columns

Size (mm) Particle Size (µm) Pressure LimitPL-SCX1000Å

PL-SCX4000Å

1.0 x 50 5 207 bar, 3000 psi PL1345-1502 PL1345-15032.1 x 50 5 207 bar, 3000 psi PL1945-1502 PL1945-15034.6 x 50 5 207 bar, 3000 psi PL1545-1502 PL1545-15032.1 x 50 8 207 bar, 3000 psi PL1945-1802 PL1945-18032.1 x 150 8 207 bar, 3000 psi PL1945-3802 PL1945-38034.6 x 50 8 207 bar, 3000 psi PL1545-1802 PL1545-18034.6 x 150 8 207 bar, 3000 psi PL1545-3802 PL1545-38034.6 x 150 10 207 bar, 3000 psi PL1545-3102 PL1545-31034.6 x 250 10 207 bar, 3000 psi PL1545-5102 PL1545-510325 x 50 10 207 bar, 3000 psi PL1245-1103 PL1245-110325 x 150 10 207 bar, 3000 psi PL1245-3103 PL1245-310350 x 150 10 207 bar, 3000 psi PL1745-3103 PL1745-3103100 x 300 10 207 bar, 3000 psi PL1845-2103 PL1845-21034.6 x 150 30 207 bar, 3000 psi PL1545-3702 PL1545-37034.6 x 250 30 207 bar, 3000 psi PL1545-5703 PL1545-570325 x 150 30 207 bar, 3000 psi PL1245-3702 PL1245-370350 x 150 30 207 bar, 3000 psi PL1745-3703 PL1745-3703100 x 300 30 207 bar, 3000 psi PL1845-3102 PL1845-3103

PL-SCX Strong Cation-Exchange Bulk Media

Size Particle Size (µm)PL-SCX1000Å

PL-SCX4000Å

100 g 10 PL1445-4102 PL1445-41021 kg 10 PL1445-6102 PL1445-6103100 g 30 PL1445-4702 PL1445-47031 kg 30 PL1445-6702 PL1445-6703

412


Agilent Bio-Monolith Ion-Exchange HPLC Columns• Polymer-based, monolith HPLC columns designed for macro biomolecule separations• Flow-rate independent separations; no diffusion, no pores and no void volume make transport

between mobile and stationary phase very rapid• Monolith disk is 5.2 mm x 4.95 mm (100 µL column volume) with continuous channels, eliminating

diffusion mass transfer• Extremely fast separations speed up method development time and decrease costs; locking in

method parameters takes significantly less time and buffer

Agilent Bio-Monolith Ion-Exchange HPLC columns provide high resolution and rapid separations ofantibodies (IgG, IgM), plasmid DNA, viruses, phages and other macro biomolecules. The product familyoffers strong cation-exchange, strong and weak anion-exchange and Protein A phases. Bio-Monolith HPLC columns are compatible with HPLC and preparative LC systems, including Agilent 1100 and 1200HPLC systems.

Agilent Bio-Monolith HPLC Column Selection Guide

Column Description Key Applications Part No.Bio-Monolith QA The quaternary amine bonded phase (Strong Anion-

Exchange) is fully charged over a working pH range of 2-13, binding negatively charged biomolecules.

ü Adenovirus process monitoring and quality controlü IgM purification monitoring and quality controlü Monitoring DNA impurity removalü Monitoring endotoxin removalü HSA Purity

5069-3635

Bio-Monolith DEAE The diethylaminoethyl bonded phase (Weak Anion-Exchange) offers increased selectivity of biomoleculeswith negative charge over a working pH range of 3-9.

ü Process monitoring and quality control ofbacteriophage manufacturing and purification

ü Process monitoring and quality control of plasmidDNA purification

5069-3636

Bio-Monolith SO3 The sulfonyl bonded phase (Strong Cation-Exchange) isfully charged over a working pH range of 2-13, bindingpositively charged biomolecules.

ü Fast and high resolution analytical separations oflarge molecules such as proteins and antibodies

ü Hemoglobin A1c fast analytics

5069-3637

Bio-Monolith Ion-Exchange HPLC Column

Agilent also offers a Protein A Bio-Monolith column for affinity chromatography. For more information, see pages 434-436.

TIPS & TOOLS



Column SpecificationsDimensions 5.2 mm x 4.95 mmColumn volume 100 µLMaximum pressure 150 bar (15 MPa, 2200 psi)Temperature min/max Working: 4-40 °C

Storage: 4-30 °CRecommended pH Working range: 2-13

Cleaning-in-place: 1-14Materials of construction Hardware: Stainless steel

Packing: poly(glycidyl methacrylate-co-ethylene dimethacrylate) highly porous monolith Color ring identifier Bio-Monolith QA: Blue

Bio-Monolith DEAE: Green Bio-Monolith SO3: Red

Shelf life/expiration date SO3, QA, DEAE: 24-36 months

414


Baseline expansion of a separation of protein standardsColumn: Agilent Bio-Monolith CM15,

5.5 x 15 mmMobile Phase: A: 10 mM Na2HPO4, pH 6.0

B: A + 0.5 M NaCl or just 0.5 M Na2HPO4, pH 6.0

Flow Rate: 2 mL/min

Gradient: 0.5 min hold with mobile phase A followed by a lineargradient to 45% B in 15 min (elapsed time 15.5 min);then 60% B at 15.6 min continued to 20 min. Columnflushed with 100% B for 15 min before re-equilibration for the next run.pH Gradient: A: 5 mM Na2HPO4, buffer pH 5.5 and B:40 mM NA2HPO4 (not buffered, pH 8.9). 2% B/min at1 mL/min for 15 min, followed by a column wash with90% B for 5 min.


Sample: One mg each/mL in mobile phase A.1. RNAse from bovine pancreas (pI 9.6)2. Cytochrome c from bovine heart (pI 10.37-10.8)3. Lysozyme from chicken egg (pI 11.35) (0.5 mg)

Instrument: Agilent 1200 SL with diode array detector

4 6 8 10 12 14 16 18 min

468

101214

mAU

4

1 2 3

6 8 10 12 14 16 18 min

468

101214

mAU

4.483

4.968

6.357

6.834

7.832

9.072

12.17

0

16.41

0

4.284 4.5

204.6

884.9

45 5.653

6.482

7.059 7.6

04 8.162

9.271

10.33

5 16.90

1

A with NaCl gradient

B with Na2HPO4 gradient

B shows a better resolution of protein contaminants.

0

5

10

15

20

25

30

35

40

45

50

0

20

40

60

80

100

120

1 3

2

0 2 4 6 8 10 12

min



As phage proliferation progresses, the genomic DNA (gDNA) concentration increases as the host cells are being lysed. In the late stages offermentation, gDNA begins to degrade into fragments. These gDNA fragments cannot be easily removed by purification media, therefore it iscritical to stop the fermentation cycle prior to the degradation of the genomic DNA. The chromatogram above represents three samples takenfrom the bioreactor at 36, 158 and 191 minutes. Peak 1 represents phage, media and host cells, peak 2 the intact gDNA and peak 3 thefragmented gDNA.

Bio-Monolith DEAE column monitors phageproduction during fermentationColumn: DEAE

5069-36365.2 x 4.95 mm

Mobile Phase: A: 125 mM Phosphate buffer, pH 7.0B: 125 mM Phosphate buffer + 1 M NaCl, pH 7.0

Flow Rate: 1 mL/min

Gradient: 100% buffer A (2.5 min)0-100% buffer B (10 min)100% buffer A (2 min)


Instrument: High pressure gradient HPLC system, Agilent 1200 Infinity LC

Relat

ive A

bsor

banc

e (mA

U)

% G

radie

nt

Time: 36 minTime: 158 minTime: 191 min% Buffer B

Phages and other components

416


Size Exclusion Chromatography (SEC)Accurately determine biomolecule aggregation, fragmentation, and chemicalligation/modificationSize exclusion chromatography (SEC) is a technique for separating proteins, oligonucleotides, and othercomplex biopolymers by size using aqueous eluents.

Applying SEC to aggregation studiesThe size, type, and content of aggregates present in protein biopharmaceuticals can affect both efficacy and formulation – or worse, induce an immunogenic response. Aggregation formations occur through avariety of mechanisms, including disulfide bond formation and non-covalent interactions.

Because the size of protein aggregates, including dimers, is sufficiently different from the protein monomer,you can separate the various forms using SEC. In fact, SEC with UV or light scattering is a standardtechnique for quantifying protein aggregation.

Applying SEC to quantitation and molecular weight determinationFor proteins and other molecules of discreet molecular weight, SEC can be used to detect and quantitatemonomers, dimers, aggregates and fragments. SEC can also separate oligonucleotide mixtures.

For biopolymers of varying sizes, like starches and other polysaccharides, SEC can provide data onmolecular weight distribution and branching (with the proper detectors).



As a leading manufacturer of SEC columns and instruments for over 30 years, Agilent is continuallydeveloping new SEC products that will provide even higher resolution and quicker separations. This sectionhighlights Agilent’s broad family of SEC columns for protein biopolymer analysis:

• Bio SEC-3 and Bio SEC-5 columns are available in a variety of pore sizes, and are well suited forprotein analysis – especially when determining the presence of dimers and aggregates in therapeuticbiologicals. Note that 3 µm Bio SEC-3 columns provide higher resolution than our industry-standard 5 µm Bio SEC-5 columns.

• ProSec 300S columns work well with globular proteins under high salt conditions.• ZORBAX GF-250 and GF-450 columns are best for preparative SEC of proteins, because of their

larger column size and higher flow rates.• PL aquagel-OH columns can be used to analyze biopolymers of broad molecular weights, such as

PEGs, oligo- and polysaccharides, starches, and gums.

Size Exclusion Chromatography (SEC)

Application Agilent Columns NotesPeptides, proteins Agilent Bio SEC-3 Higher resolution and faster separations from 3 µm particles, with 100Å,

150Å, and 300Å pore sizes.Large biomolecules and sampleswith multiple molecular weightcomponents

Agilent Bio SEC-5 More pore size options (100Å, 150Å, 300Å, 500Å, 1000Å, and 2000Å) to cover a wider range of analytes.

Globular proteins, antibodies ProSEC 300S Single column option for protein analysis in high salt conditions.Proteins, globular proteins ZORBAX GF-250/450 Higher flow rate capabilities and larger column size for SEC semi-prep

and prep.Low MW polymers and oligomers,oligosaccharides, PEGs,lignosulfonates

2 or 3 PL aquagel-OH The PL aquagel-OH analytical series has a pH range of 2-10, compatibility with organic solvent (up to 50% methanol), mechanicalstability up to 140 bar (2030 psi), and low column operating pressures.ü PL aquagel-OH 8 µm

ü PL aquagel-OH 20 5 µmü PL aquagel-OH MIXED-M 8 µm

Polydisperse biopolymers,polysaccharides, cellulosederivatives

2 or 3 PL aquagel-OHü PL aquagel-OH MIXED-H 8 µmü PL aquagel-OH 60/50/40 8 µm

Very high MW polymers, hyaluronic acids, starches, gums


418


Agilent Bio SEC-3• Exceptional loading capacity, stability, and reproducibility for size-based biomolecule separations• Sharper peaks, higher resolution, and better protein recovery• Faster separations than large-particle SEC columns• Compatibility with most aqueous buffers• Excellent stability in high-salt and low-salt conditions

Agilent Bio SEC-3 HPLC columns are a breakthrough technology for size exclusion chromatography (SEC).They are packed with spherical, narrowly dispersed 3 µm silica particles coated with a proprietaryhydrophilic layer. This thin polymeric layer is chemically bonded to pure, mechanically stable silica undercontrolled conditions, ensuring a highly efficient size exclusion particle.

Agilent Bio SEC-3 HPLC columns are available in 100Å, 150Å and 300Å pore sizes to accommodate mostpeptide and protein size exclusion separations.


Pore Size Particle Size MW Range pH Range Max Pressure Flow Rate100Å 3 µm 100-100,000 2-8.5 240 bar, 3500 psi 0.1-1.25 mL/min (7.8 mm id)

0.1-0.4 mL/min (4.6 mm id)150Å 3 µm 500-150,000 2-8.5 240 bar, 3500 psi 0.1-1.25 mL/min (7.8 mm id)

0.1-0.4 mL/min (4.6 mm id)300Å 3 µm 5,000-1,250,000 2-8.5 240 bar, 3500 psi 0.1-1.25 mL/min (7.8 mm id)

0.1-0.4 mL/min (4.6 mm id)

TIPS & TOOLS

Deactivated/silanized vials have inert surfaces that will not interact with metals, biologicals or proteins, andwill not cause pH shifts. Avoid standard polypropylene vials for biological or light-sensitive compounds.

VLC_MD_Mab

0

50

100

150

200

250

300

mAU

4 6 8 10 12 14 min



Calibration curves – Bio SEC-3Column: Bio SEC-3

7.8 x 300 mm, 3 µmMobile Phase: 150 mM Na phosphate, pH 7.0


Detector: UV

Proteins MWt 300Å 150Å 100Å

Thyroglobulin 670000 6.34 5.50 5.63

Gamma globulin 158000 8.03 6.24 5.74

BSA 67000 8.90 7.00 6.03

Ovalbumin 45000 9.57 7.70 6.41

Myoglobin 17000 10.12 8.50 7.10

Ribonuclease A 12700 10.40 8.80 7.46

Vitamin B-12 1350 11.90 11.40 10.20

MWvsRet

4100

1,000

10,000

100,000

1,000,000

10,000,000

100,000,000

1,000,000,000

5 6 7 8 9 10 11 12 13

300Å150Å100Å

Mole

cular

Weig

htRetention Volume (mL)

Intact MAb monomer and dimer separationColumn: Bio SEC-3, 300Å

5190-25117.8 x 300 mm, 3 µm

Buffer: Sodium phosphate buffer, pH 7.0, 150 mM

Isocratic: 0-100% Buffer A from 0-30 min


Sample: CHO-humanized MAb, 5 mg/mL – intact

Injection: 5 µL

Detector: UV 220 nm


Monomer

Dimer

420


Comparison of Agilent Bio SEC-3 and competitor column in the analysis of a monoclonal antibodyColumn: Bio SEC-3, 300Å

5190-25117.8 x 300 mm, 3 µm

Column: Competitor 7.8 x 300 mm

Mobile Phase: 150 mM sodium phosphate + 100 mM Na sulfate (with salt)150 mM sodium phosphate (without salt)



Sample: MAb (2 mg/mL)Mono_Dimer1

0 2 4 6 8 10 min

8 minutes8 minutes 0

10

40mAU

20

30

0 2 4 6 8 10 min

0

10

40mAU

20

30

The Agilent Bio SEC-3 column reveals the presence of smaller MW species missed by the competitor column.

Agilent Bio SEC-3 Competitor column

Monomer

DimerWith salt

Without salt

Monoclonal Antibody Monomer and Dimer Analysis using Agilent Bio SEC-3 and a Competitor Column

Eluent ColumnResolution RatioMonomer:Dimer

MonomerEfficiency

PercentageDimer

With salt Agilent 2.04 7,518 0.59With salt Competitor 1.88 3,967 0.59Without salt Agilent 2.08 7,942 0.60Without salt Competitor 1.92 4,164 0.57

Monomer

DimerWith salt

Without salt



Pore Size Choice

The choice of media pore size will influence the resolution in SEC. As the separation is based on differences in molecular size in solution, the samplemust be able to permeate the porous structure of the particles – if the pore size is too small, the samples will be excluded from the pores and elutein the void volume of the column, and if too large then, all will be able to fully permeate the particles and so there will be very little separation.

Pore size choice: ProteinsColumn A: Bio SEC-3, 100Å

5190-25034.6 x 300 mm, 3 µm

Column B: Bio SEC-3, 150Å5190-25084.6 x 300 mm, 3 µm

Column C: Bio SEC-3, 300Å5190-25134.6 x 300 mm, 3 µm

Mobile Phase: 50 mM Na2HPO4, 50 mM NaH2PO4 +0.15 M NaCl, pH 6.8



Sample: BioRad Gel Filtration Standards Mix

PoreSz_Proteins

0 2.5

100Å

150Å

300Å 1

2

3

4

56

7

5.0 7.5 10.0 12.5 15.0 17.5 20.0

0

500

1000

1500

2000

2500mAU

Pore size choice: Mouse IgGColumn A: Bio SEC-3, 100Å

5190-25034.6 x 300 mm, 3 µm

Column B: Bio SEC-3, 150Å5190-25084.6 x 300 mm, 3 µm

Column C: Bio SEC-3, 300Å5190-25134.6 x 300 mm, 3 µm

Mobile Phase: 50 mM Na2HPO4, 50 mM NaH2PO4 +0.15 M NaCl, pH 6.8



Sample: Mouse IgG

PoreSz_Mouse

0 2.5 5.0 7.5 10.0 12.5 15.0 17.5 20.0

0

200

800

1000

1200

1400

1

2

3

4

300Å

150Å

100Å

mAU

400

600

1. Dimer2. Monomer3. Monomer Fragment4. Azide

1. Thyroglobulin Aggregates2. Thyroglobulin3. IgA4. g-globulin5. Ovalbumin6. Myoglobin7. Vitamin B12

422


Column Length

Where the separation time is a critical parameter, shorter columns packed with the higher efficiency, 3 µm media are used. With the shortercolumns, higher flow rates are used to reduce the analysis time but without compromising the quality of the data – quantitation of monoclonalantibody monomer and dimer.

150 mm 300 mm

Dimer

1.5 mL/min 1.0 mL/min

4 min

Monomer

DimerWith salt

Without salt

Agilent Bio SEC-3 column length comparison,150 mmColumn: Bio SEC-3, 300Å

5190-25127.8 x 150 mm, 3 µm

Mobile Phase: 150 mM sodium phosphate

Flow Rate: 1.0 mL/min (56 bar), 1.5 mL/min (75 bar)


Sample: MAb (2 mg/mL)

Agilent Bio SEC-3 column length comparison,300 mmColumn: Bio SEC-3, 300Å

5190-25117.8 x 300 mm, 3 µm

Mobile Phase: 150 mM sodium phosphate + 100 mM Na sulfate(with salt)150 mM sodium phosphate (without salt)



Sample: MAb (2 mg/mL)

8 min

Monomer

Dimer

Monomer



Agilent Bio SEC-3

Size (mm) Particle Size (µm)

Bio SEC-3100ÅUSP L33



7.8 x 300 3 5190-2501 5190-2506 5190-25117.8 x 150 3 5190-2502 5190-2507 5190-25124.6 x 300 3 5190-2503 5190-2508 5190-25134.6 x 150 3 5190-2504 5190-2509 5190-25147.8 x 50, Guard 3 5190-2505 5190-2510 5190-2515

424


Agilent Bio SEC-5• Maximum recovery for a broad range of size-based, biomolecule separations• Outstanding reproducibility and column lifetime• Excellent stability, even under high-pH, high-salt, and low-salt conditions• Compatibility with most aqueous buffers

Agilent Bio SEC-5 HPLC columns are packed with 5 µm silica particles coated with a proprietary, neutral,hydrophilic layer for maximum efficiency and stability. Our specially designed packing also provides highpore volume, improving both peak capacity and resolution.

Bio SEC-5 columns are available in 5 µm particles with 100Å, 150Å, 300Å, 500Å, 1000Å, and 2000Ånominal pore sizes.


Pore Size Particle Size MW Range pH Range Max Pressure Flow Rate100Å 5 µm 100-100,000 2-8.5 240 bar, 3500 psi 0.1-1.25 mL/min (7.8 mm id)

0.1-0.4 mL/min (4.6 mm id)150Å 5 µm 500-150,000 2-8.5 240 bar, 3500 psi 0.1-1.25 mL/min (7.8 mm id)




0.1-0.4 mL/min (4.6 mm id)2000Å 5 µm >10,000,000 2-8.5 240 bar, 3500 psi 0.1-1.25 mL/min (7.8 mm id)

0.1-0.4 mL/min (4.6 mm id)



Calibration curves – Bio SEC-5Column: Bio SEC-5

7.8 x 300 mm, 5 µmMobile Phase: 150 mM Na phosphate, pH 7.0



4100

1,000

10,000

100,000

1,000,000

10,000,000

100,000,000

1,000,000,000

5 6 7 8 9 10 11 12 13CalCurves_SEC5

Mole

cular

Weig

ht

Retention Volume (mL)

1000Å500Å300Å150Å100Å

Side-by-side comparison

Separation of a protein mixture on an Agilent Bio SEC-5 HPLCcolumn and a Tosoh TSK-Gel column. Notice the sharper peaks and better resolution on the Agilent Bio SEC-5 HPLC column.

1. Thyroglobulin, 5.43 min2. BSA dimer, 6.19 min3. BSA monomer, 6.93 min4. Ribonuclease A, 8.74 min5. Poly-DL-alanine (1-5 kDa), 9.90 min6. Uracil, 12.13 min

1. Thyroglobulin, 5.64 min2. BSA dimer, 6.23 min3. BSA monomer, 7.02 min4. Ribonuclease A, 9.22 min5. Poly-DL-alanine (1-5 kDa), 10.02 min6. Uracil, 11.81 min

Agilent Bio SEC-5, 150Å

TSK G2000SWxl

Column: Bio SEC-55190-25217.8 x 300 mm, 5 µm

Mobile Phase: 150 mM Na phosphate, pH 7.0



Proteins MW

Retention Volume

1000Å 500Å 300Å 150Å 100Å

Thyroglobulin 670000 10.07 8.23 7.03 5.82 5.77

Gamma globulin 158000 10.88 9.80 8.57 6.55 5.79

BSA 67000 11.13 10.44 9.44 7.29 6.00

Ovalbumin 45000 11.28 10.83 9.89 7.90 6.40

Myoglobin 17000 11.44 11.28 10.42 8.66 7.05

Ribonuclease A 12700 11.52 11.41 10.58 8.93 7.32

Vitamin B-12 1350 12.00 12.59 11.78 11.49 10.30

Mono_Antibody

0 2 4 6

12 3

1 2

3

8 10 12 14 min

0

20

80

100

120

mAU

16 18

40

60

426


Exceptional lifetime, and lot-to-lot reproducibilityColumn: Bio SEC-5, 150Å

5190-25217.8 x 300 mm, 5 µm

Mobile Phase: 150 mM PhosphateBuffer, pH 7.0

1

2 3

4

1

2

3 4

Lot 1

Lot 2

Lot 3

min min 0 2 4 6 8 10 12 14

AU

.10

.20

.30

.40

.50

.60

.70

.80

.00

0 2 4 6 8 10 12 14

After 300 injections3rd run

1. Thyroglobulin2. BSA3. Ribonuclease A4. Uracil

The four protein mixture showsexcellent retention timereproducibility over 300 injectionsand on three columns fromdifferent manufacturing lots.

Comparison between Agilent Bio SEC-3 and Agilent Bio SEC-5

Analysis of monoclonal antibodyColumn: Bio SEC-3, 300Å

5190-25117.8 x 300 mm, 3 µm

Column: Bio SEC-5, 300Å5190-25267.8 x 300 mm, 5 µm

Mobile Phase: 150 mM Sodium Phosphate, pH 7

Flow Rate: 1 mL/min

Detector: UV @ 220 nm

Sample: Humanized monoclonal antibody

1. Dimer2. Monomer3. Monomer fragment

The 3 µm column gives better separation

3 µm

5 µm

ReproducibilityLifetime



Agilent Bio SEC-5


(µm)







7.8 x 300 5 5190-2516 5190-2521 5190-2526 5190-2531 5190-2536 5190-25417.8 x 150 5 5190-2517 5190-2522 5190-2527 5190-2532 5190-2537 5190-25424.6 x 300 5 5190-2518 5190-2523 5190-2528 5190-2533 5190-2538 5190-25434.6 x 150 5 5190-2519 5190-2524 5190-2529 5190-2534 5190-2539 5190-25447.8 x 50, Guard 5 5190-2520 5190-2525 5190-2530 5190-2535 5190-2540 5190-2545

The Agilent rack can be used to optimize your 1290 Infinity LC for ultra-low dispersion, which can enhanceperformance of high-efficiency columns. Further information can be found in application note 5990-9502ENat www.agilent.com/chem/library

TIPS & TOOLS

428


ProSEC 300S• Mechanically robust silica particles that do not bleed during use• Single column with extended linear resolving range• Column dimensions for use with multi-detector systems

The Agilent ProSEC 300S column is specifically designed as a single column solution for globular proteinanalysis. The pore size selection and optimization provides an extended linear resolving range so that thissingle column can be used for analysis across the full range of globular proteins.

The particles are extremely robust and do not fragment during use to leach particulates. This givesexceptionally stable baselines making this column an ideal choice for use with light scattering detectors.

Two column dimensions, 7.5 mm id and 4.6 mm id, to suit multi-detector size exclusion chromatographyprovide an option for the analysis of small masses.

ProSEC 300S Column Specifications


ParticleSize

Protein MWRange

pHRange Flow Rate Max Pressure

ProSEC 300S 300Å 5 µm 1,500-800,000 2-7.5 <1.5 mL/min(7.5 mm id)

250 bar, 3700 psi

<0.5 mL/min(4.6 mm id)

ProSEC 300SDimensions Particle Size (µm) Part No.4.6 x 250 5 PL1547-55017.5 x 300 5 PL1147-6501Guard Columns4.6 x 50 5 PL1547-15017.5 x 50 5 PL1147-1501

5 7 9 10Retention time (min) PSEC300Sglob

133

3.5

4

4.5

5

5.5

6

Log

M



Calibration of the ProSEC 300S columnwith globular proteinsMobile Phase: 50 mM KH2PO4-K2HPO4 (@ pH 6.8)

containing 0.3 M NaCl



Sample: Protein samples

Molecular weights of the proteinsMw/Daltons Protein670,000 Thyroglobulin155,000 g-Globulin66,430 Bovine serum albumin44,287 Ovalbumin29,000 Carbonic anhydrase16,700 Myoglobulin12,384 Cytochrome c1,423 Bacitracin

Analysis of Bovine Serum Albumin by lightscattering using ProSEC 300S columnsColumn: ProSEC 300S

PL1147-65017.5 x 300 mm, 5 µm

Mobile Phase: Water + 120 mM NaCl, 2.7 mM KCI, 10 mMNaH2PO4


Detector: Differential refractive index + PL-GPC 50 Dual AngleLight Scattering Detector

Sample: Bovine serum albumin

Molecular WeightsMonomer 66,900 Daltons, 88.5%Dimer 34,900 Daltons (2.02 x monomer

molecular weight), 9.8%Trimer 197,000 Daltons (2.94 x monomer

molecular weight), 1.2%Tetramer 279,300 Daltons (5.17 x monomer

molecular weight), 0.5%0

BovineSerAlb

14

Resp

onse

Retention time (min)

Overlay of differential refractive index and dual angle light scattering sample.

Aggregation

TetramerTrimer Dimer

Monomer

RI

15 Deg

90 Deg

430


Overlay of UV and light scattering 90° for a sample of g-globulins, illustrating monomer,dimer, and trimer peaksColumn: ProSEC 300S

PL1147-65017.5 x 300 mm, 5 µm

Mobile Phase: 0.1 M KH2PO4 containing 0.3 M NaCl, pH 8.0


Temperature: 5 °C

Detector: UV at 310 nm + PL-GPC 50 Dual Angle Light Scattering Detector

Sample: Proteins UV_Overlay

Resp

onse

(mV)


UV

LS 90°

Overlay of UV and light scattering 90° for asample of BSA, illustrating monomer, dimer,trimer and aggregate peaksColumn: ProSEC 300S

PL1147-65017.5 x 300 mm, 5 µm

Mobile Phase: 0.1 M KH2PO4 containing 0.3 M NaCl, pH 8.0


Temperature: 5 °C

Detector: UV at 310 nm + PL-GPC 50 Dual Angle Light Scattering Detector

Sample: Proteins UV_Overlay_BSA

Resp

onse

(mV)


UV

LS 90°



ZORBAX GF-250 and GF-450 Gel Filtration Columns• High efficiency and reproducibility with short analysis time• Semi-prep and prep column dimensions• Compatible with organic modifiers and denaturants• Wide usable pH range (3-8)

Agilent ZORBAX GF-250 and GF-450 size exclusion (gel filtration) columns are ideal for size separations ofproteins and other biomolecules. The separation range is 4,000-900,000 for globular proteins when usingGF-250 and GF-450 columns in series. The GF-250/GF-450 size exclusion columns have a hydrophilic diolbonded phase for high recovery of proteins (typically >90%) and a unique zirconia modification of the silicafor a pH operating range from 3-8. The GF-250 and GF-450 columns are packed with precisely sized poroussilica microspheres with narrow pore size and particle size distributions. The result is a highly efficient,rugged and reproducible size exclusion column that can be used for both analytical and preparativeseparations of proteins with flow rates of up to 3 mL/min. These columns are compatible with organicmodifiers (<25%) and denaturants in the mobile phase to reduce protein aggregation. Some commonapplications include separations of protein monomers, dimers and aggregates, desalting, protein molecularweight estimation and separations of modified proteins.


Bonded Phase Pore Size Particle Size MW Range Surface Area pH Range Flow Rate Max PressureZORBAX GF-250 150Å 4 µm 4,000-400,000 140 m2/g 3.0-8.0 <3.0 mL/min 350 barZORBAX GF-450 300Å 6 µm 10,000-900,000 50 m2/g 3.0-8.0 <3.0 mL/min 350 bar


GF-250 Gel Filtration Columns

432


Retention volume versus log (MW) for the Bio-Rad standards separated on an Agilent ZORBAX GF-250 columnColumn: ZORBAX GF-250

884973-9019.4 x 250 mm, 4 µm

Mobile Phase: 200 mM Sodium phosphate, pH 7.0



Retention volume (mL)Lo

g (M

W)

Thyroglobulin (670 kDa)

Gamma globulin (158 kDa)

Ovalbumin (44 kDa)Myoglobulin (17 kDa)

Vitamin B12 (1.35 kDa)

0

12

3 4

5 6

1

2

3 4

56

5 10 15

0 5 10 15Retention time (min)

ZORBAX GF-250

ZORBAX GF-450

1. Thyroglobulin2. Catalase3. BSA4. ß-Lactoglobulin B5. Myoglobin6. Tyr-Gly-Gly

Separations of proteins on preparative columnsColumn: ZORBAX GF-250

884973-9019.4 x 250 mm, 4 µm

Column: ZORBAX GF-450884973-9029.4 x 250 mm, 6 µm

Mobile Phase: 0.2 M Na2HPO4, pH 7.0



Sample: 200 µL



ZORBAX GF-250 (USP L33) and GF-450 (USP L35) Gel Filtration Columns


(µm) Part No.GF-250, 150Å 9.4 x 250 4 884973-901GF-250, 150Å 4.6 x 250 4 884973-701GF-450, 300Å 9.4 x 250 6 884973-902

Guard Columns (hardware required)GF-250 Diol, Guard Cartridge, 2/pk 9.4 x 15 6 820675-111GF-250 Diol, Guard Cartridge, 4/pk 4.6 x 12.5 6 820950-911GF-450 Diol, Guard Cartridge, 2/pk 9.4 x 15 6 820675-111GF-250 Diol, Guard Cartridge, 4/pk 4.6 x 12.5 6 820950-911Prep Guard Hardware Kit 840140-901Guard Hardware Kit 820999-901

PrepHT ColumnsPrepHT GF-250, 150Å 21.2 x 250 6 877974-901PrepHT GF-450, 300Å 21.2 x 250 6 877974-910PrepHT Endfittings, 2/pk 820400-901PrepHT GF-250, Guard Cartridge, 2/pk 17.0 x 7.5 5 820212-911PrepHT GF-450, Guard Cartridge, 2/pk 17.0 x 7.5 5 820212-911Guard Cartridge Hardware 820444-901

434


Affinity ChromatographyAffinity chromatography is a powerful technique which takes advantage of highly specific molecularinteractions, frequently between specific proteins (e.g. antigen/antibody). Agilent offers several specialtyaffinity products, a monolithic Protein A column for the isolation and quantitation of IgG and a series ofMultiple Affinity Removal Systems for the elimination of high abundance proteins in biological samples.

Agilent Bio-Monolith Protein A HPLC Columns• Designed for the analytical separation of all IgG (human and mouse), except for IgG class3• Flow-rate independent separations; no diffusion, no pores and no void volume make transport

between mobile and stationary phase very rapid• Extremely fast separations speed up method development time and decrease costs• Locking in method parameters takes significantly less time and buffer

Agilent Bio-Monolith Protein A HPLC columns are part of the Agilent Bio-Monolith column family. Protein A Bio-Monolith columns are compatible with HPLC and preparative LC systems, including Agilent 1100 and 1200 HPLC systems.

TIPS & TOOLS

For information on Ion-Exchange Bio-Monolith columns, turn to pages 412-415.

Bio-Monolith Protein A Column, 5069-3639



Bio-Monolith Protein AColumn Description Key Applications Part No.Bio-Monolith Protein A The Protein A affinity column is designed for the

analytical separation of all IgG (human and mouse),except for IgG class3.

ü Quantitative determination of IgG (fermentation titercalculation)

5069-3639

TIPS & TOOLS

Further information can be found inthe following application note:

Rapid Human Polyclonal IgGQuantification Using the Agilent Bio-Monolith Protein A HPLC Column (publication # 5989-9733EN)


Column SpecificationsDimensions 5.2 mm x 4.95 mmColumn volume 100 µLMaximum pressure 150 bar (15 MPa, 2200 psi)Temperature min/max Working: 4-40 °C

Storage: 4-30 °CRecommended pH Working range: 2-13

Cleaning-in-place: 1-14Materials of construction Hardware: Stainless steel

Packing: poly(glycidyl methacrylate-co-ethylene dimethacrylate) highlyporous monolith

Color ring identifier Bio-Monolith Protein A: WhiteShelf life/expiration date Protein A: 12 months

436


Rapid human polyclonal IgG quantification usingthe Agilent Bio-Monolith Protein A HPLC columnColumn: Protein A

5069-36395.2 x 4.95 mm

Mobile Phase: PBS buffer, pH 7.40.5 M acetic acid, pH 2.6

Flow Rate: 1 mL/min

Gradient: Stepwise gradient: 100% bufferA-100% buffer B-100% buffer A (0.5 min each step)

Detector: A high pressure gradient HPLC system, Agilent 1200 Infinity LC - UV at 280 nm

Sample: Human Plasma diluted with binding buffer (PBSbuffer, pH 7.4)

0

200

400

600

800

1000

1200

0 0.5 1 1.5 2 2.5 30

20

40

60

80

100

120

Relat

ive ab

sorb

ance

[mAU

]

Time [min]

% G

radie

nt

SDS PAGE analysis of fractions from the separation.

The selectivity of the Bio-Monolith Protein A column for the IgG from human plasma. IgG binds to protein A, a 100% buffer B step gradient is applied, and IgG elutes at 1.5 min.

Key:

Lane 1: Whole serum prior to separation

Lane 2: IgG standard

Lane 3: Peak 1 (flow-through fraction)

Lane 4: Peak 2 (Protein A-bound fraction; i.e. IgG1 and IgG2)



Agilent Protein Fractionation System and Proteomics Reagents• LC/MS analysis of biological samples• Preparation for electrophoretic analysis• Sample preparation for biomarker discovery• Instrument and workflow validation• Cost-effective immunodepletion• Sample desalting, concentration, and fractionation

In order to more easily isolate and identify proteins in biological samples, such as serum, plasma, andcerebro-spinal fluid (CSF), the Agilent Multiple Affinity Removal System is designed to chromatographicallyeliminate interfering high-abundance proteins from biological samples. Removal of these abundant proteinsimproves the subsequent LC/MS and electrophoretic analysis of the sample by effectively expanding thedynamic range.

For sample fractionation and desalting, the Agilent mRP-C18 High-Recovery Protein column is designed tosimultaneously desalt, concentrate, and fractionate in one easy step with extremely high recovery ofsamples as compared to conventional RP HPLC columns that are fully compatible with LC/MS analysis.

In addition, validated reagents for sample preparation in biomarker discovery and other proteomicsapplications are also available, including a complex standard, and proteomics grade trypsin. For yourconvenience, these reagents are fully compatible with Agilent LC/MS methods and require no additionalsample pretreatments.

Large volume requirements and custom column dimensions can also be addressed with our custom configurations.

438


Multiple Affinity Removal SystemThe Multiple Affinity Removal System from Agilent enables the identification and characterization of high-value, low abundant proteins and biomarkers found in serum, plasma, and other biological fluids.

The Multiple Affinity Removal System reproducibly and specifically removes up to 14 high abundantproteins found in human biological fluids and 3 high abundant proteins found in mouse biological fluids.

The Multiple Affinity Removal System is available in a variety of LC column dimensions and in spin cartridgeformat. When combined with Agilent's optimized buffers, convenient spin filters and concentrators, theAgilent Multiple Affinity Removal System creates an automated, integrated depletion solution compatiblewith most LC instruments (columns), and bench top centrifuges (spin cartridges).

Samples depleted using the Multiple Affinity Removal System are ready for downstream analyses such as2-D gel electrophoresis, LC/MS, and other analytical techniques.

Multiple Affinity Removal System



Multiple Affinity Removal System Selection Guide

Product Proteins RemovedTotal Protein

Removed Dimension Load Capacity Part No.MARS Human-14 Albumin, IgG, antitrypsin, IgA, transferrin,

haptoglobin, fibrinogen, alpha2-macroglobulin, alpha1-acid glycoprotein,IgM, apolipoprotein Al, apolipoprotein All,complement C3, transthyretin

94% Spin Cartridge 8 - 10 µL 5188-65604.6 x 50 mm 20 µL 5188-6557

4.6 x 100 mm 40 µL 5188-655810.0 x 100 mm 250 µL 5188-6559

MARS Human-7 Albumin, IgG, IgA, transferrin, haptoglobin,antitrypsin, fibrinogen

88-92% Spin Cartridge 12 - 14 µL 5188-64084.6 x 50 mm 30 - 35 µL 5188-6409

4.6 x 100 mm 60 - 70 µL 5188-641010.0 x 100 mm 250 - 300 µL 5188-6411

MARS Human-6 Albumin, IgG, IgA, transferrin, haptoglobin,antitrypsin


4.6 x 100 mm 30 - 40 µL 5185-5985MARS Human-6High Capacity

Albumin, IgG, IgA, transferrin, haptoglobin,antitrypsin


4.6 x 100 mm 60 - 80 µL 5188-533310.0 x 100 mm up to 340 µL 5188-5336

MARS Human-2 Albumin, IgG 69% Spin Cartridge 50 µL 5188-88254.6 x 50 mm 100 µL 5188-8826

MARS Human-1 Albumin 50-55% Spin Cartridge 65 µL 5188-53344.6 x 50 mm 130 µL 5188-6562

MARS Mouse-3 Albumin, IgG, transferrin 80% Spin Cartridge 25 - 30 µL 5188-52894.6 x 50 mm 37 - 50 µL 5188-5217

4.6 x 100 mm 75 - 100 µL 5188-5218

440


Illustration of high abundance proteins removed by Agilent Multiple Affinity RemovalColumns and Spin Cartridges

Transferrin

Fibrinogen

IgA

Haptoglobin

a1-Antitrypsin

IgG

Albumin

15%

Complement C3

a1-Acid Glycoprotein

a2-Macroglobulin

6% Remaining for Analysis

Apolipoprotein AI

Apolipoprotein AII

IgM

Transthyretin

TIPS & TOOLS

Learn more about Agilent’s complete services portfolio at www.agilent.com/chem/services

Luer-Lok syringe, 5188-5250



LC Column Reagent Starter Kit, 5185-5986

Multiple Affinity Removal System Starter KitsThe LC Column and Spin Cartridge Reagent Starter Kits include all the required supplies to use with Multiple Affinity Removal System. These buffers provide optimal conditions for column longevity and sample reproducibility.

• The kits provide enough Buffer A and Buffer B for approximately 200 sample depletions using the 4.6 x 50 mm LC columns, approximately 100 sample depletions using the 4.6 x 100 mm LC columnsand 200 spin cartridge uses.

• Buffer A, the loading buffer, minimizes protein-protein interactions, allowing low abundant proteinsoften bound to high abundant proteins to pass through the column, while the targeted high abundantproteins bind to their associated antibodies.

• Buffer B, the elution buffer, then disrupts the antibody-protein interaction eluting the high abundantproteins off the column.

Multiple Affinity Removal System Starter KitsDescription Part No.LC Column Reagent Starter KitIncludes:

5185-5986

Buffer A, 1 L, for loading, washing, and equilibrating, qty 2 5185-5987Buffer B, 1 L, for eluting 5185-59880.22 µm cellulose acetate, 25/pk, qty 2 5185-5990Spin concentrators, 5K MWCO, 4 mL, 25/pk 5185-5991

Multiple Affinity Removal Spin Cartridge Reagent KitIncludes:

5188-5254

Buffer A, 1 L, for loading, washing, and equilibrating 5185-5987Buffer B, 1 L, for eluting 5185-5988Spin filters, 0.22 µm cellulose acetate, 25/pk, qty 2 5185-5990Spin concentrators, 5K MWCO, 4 mL, 25/pk 5185-5991Luer-Lok adapters, 2/pk 5188-5249Plastic syringe, 5 mL, Luer-Lok, 2/pk 5188-5250Microtube, 1.5 mL, screw top, 100/pk, qty 6 5188-5251Caps and plugs, 6/pk 5188-5252PTFE needles, Luer-Lok, 10/pk 5188-5253

High concentration sample dilution buffer, 50 mL 5188-8283

Luer-Lok adapters, 5188-5249

Luer-Lok needles, 5188-5253

442


mRP-C18 High-Recovery Protein ColumnsThe mRP (macroporous reversed-phase) C18 High-Recovery Protein column is designed for high recovery,high resolution separation, fractionation, and simultaneous desalting of complex protein samples (likeimmunodepleted serum or plasma proteins).

mRP-C18 High-Recovery Protein ColumnsDescription Protein Load Capacity Part No.mRP-C18, 0.5 x 100 mm 10 ng - 5 µg 5188-6510mRP-C18, 2.1 x 75 mm 8 - 85 µg 5188-6511mRP-C18, 4.6 x 50 mm 40 - 380 µg 5188-5231

Proteomics Reagents for LC/MS AnalysisThe Agilent Complex Proteomics Standard is a soluble Pfu protein extract containing over 1,500 proteins.Together with our TPCK-treated proteomics grade trypsin this is an ideal combination for workflow validationin LC/MS biomarker discovery and other proteomic studies.

Proteomics Reagents for LC/MS AnalysisDescription Part No.Complex Proteomics Standard 400510Proteomics Grade Trypsin 204310

• Greater than 95-99% protein sample recovery has been observed with immunodepleted serum using the Agilent Multiple Affinity Removal System – LC column

• Can load up to 380 µg of total protein mass without reducing chromatographic resolution of the proteins

• Column packed with macroporous C18-bonded ultrapure 5 µm particle silica designed to reduce or eliminate strong adsorption of proteins

• Maximum operating pressure of 250 bar (4000 psi)• Compatible with water and all common organic solvents

mRP-C18 High-Recovery Protein Column, 4.6 x 50 mm, 5188-5231



Protein Fractionation of Complex Samples on the mRP Column

MRPC18

Time (min)0

1

2

3

4

5

6

7mAU

10 20 30 40 50 60 70 80Time (min)

0012345678

mAU

10 20 30 40 50 60

Time (min)0

0

5

10

15

20

25mAU

10 20 30 40 50Time (min)

00

510152025

mAU

10 20 30 40 50 60

HeLa Cell Lysate (352 µg)

"Top-6" Depleted Human Serum Human Brain Membrane Lipid Raft Prep (500 µg)

HeLa Membrane Prep Highest Recovery

mRP-C18, 4.6 x 50 mm

Lipids

mRP-C18 High-Recovery Protein Column, 0.5 x 100 mm, 5188-6510

444


Method DevelopmentZORBAX Column MethodsThis ZORBAX Column Selection Strategy for Proteins and Peptides provides some critical details on method development for proteins or polypeptides.

Peptides, Polypeptides, ProteinsMW <50 kDa

Initial Bonded Phase

StableBond 300SB-C8

300SB columns are wide-pore columns with unbeatable lifetime inTFA-containing mobile phases. This makes them an ideal first choicefor separations of peptides and proteins.

• C8 is an excellent starting bonded phase because of its moderatehydrophobicity

• C18 and C8 are generally selected for peptides and proteindigests but can also be used for proteins

• C3, C4 and CN are generally selected for larger, hydrophobicpolypeptides and proteins but can also be used for peptides

• PLRP-S when chemical and thermal stability are needed

Initial Separation Conditions

Mobile Phase: A: 95% H2O: 5% ACN with 0.1% TFAB: 5% H2O: 95% ACN with 0.085% TFA


Temperature: 35-40 °C

Flow Rate: 1 mL/min

Peptides, Polypeptides, ProteinsMW >50 kDa

Choose the Initial Column and Conditions for Peptides, Polypeptides, and Proteins

StableBond 300SB-C8 4.6 x 150 mm, 3.5 or 5 µm883995-906863973-906

Column:

Poroshell 300SB-C18

Poroshell 300SB columns use an innovative particle technology todeliver rapid protein separations. Short anaysis times with efficientpeaks are easily obtained with Poroshell columns.

• C18 is a good starting bonded phase choice with Poroshell formost peptides, polypeptides and proteins because the retention is maximized

• C8 is generally selected for moderate size proteins but can beused with polypeptides or very large proteins

• C3 is generally selected for antibodies or large proteins but canbe used for peptides and polypeptides

Column: Poroshell 300SB-C18 2.1 x 75 mm, 5 µm 660750-902

Mobile Phase: A: 95% H2O: 5% ACN with 0.1% TFAB: 5% H2O: 95% ACN with 0.085% TFA


Temperature: 35-40 °C

Flow Rate: 2 mL/min



Start at Low pH with Simple Aqueous/Organic GradientTypically, a water/acetonitrile with 0.1% TFA gradient is used to elute all components of interest. A typical high resolution gradient on a 300Å pore size column requires 30-50 min. A Poroshell column requires a shorter analysis time and a higher flow rate and still provides exceptional resolution. To improve resolution, increase the gradient time, decrease column length, or increase flow rate.

Optimize Sample SolubilityFor best peak shape and recovery at any pH, it is important to completely solubilize a sample. Highly acidic or neutral solvents can be used withZORBAX 300StableBond and Poroshell 300SB, while neutral solvents and dilute bases can be used with ZORBAX 300Extend-C18.

Solvent Choices to Solubilize Proteins and Peptides

Water/phosphate BufferDilute acid (TFA, Acetic Acid or HCI)Neutral pH, 6-8 M guanidine-HCI or isthiocyanate5% HOAc/6 M ureaDilute acid + aqueous/organic solvents (ACE, MeOH, THF)Dilute base (ammonium hydroxide)DMSO or 0.1%-1% in DMSOFormamide

StableBond 300SB - up to 80 °C

Weakest

Strongest

Poroshell 300SB - up to 80 °C

Increase the TemperatureSeparations of proteins and peptides are influenced by temperature and higher column temperature can dramatically improve both resolution andrecovery of proteins and hydrophobic and aggregating peptides.

Optimize Mobile Phase pHTry Mid and High pH if Low pH does not work

If an optimized, low pH method does not provide an ideal separation, then mid or high pH mobile phase can be used. At high pH, selectivity is oftenvery different because acidic amino acids become negatively charged and some basic amino acids may lose their charge. ZORBAX 300Extend-C18 is an excellent choice for mid to high pH separation.

Column: ZORBAX 300Extend-C18 4.6 x 150 mm, 5 µm773995-902

Mobile Phase: A: 20 mM NH4OH in H2OB: 20 mM NH4OH in 80% ACN


Temperature: 25-30 °C (<60 °C)

Flow Rate: 1 mL/min

446


Starting Column Choices for Analytical Separations of Peptides, Polypeptides, and Proteins

Low pH Mid and High pH

MW <50 kDaZORBAX 300SB-C8

4.6 x 150 mm, 3.5 µm863973-906

MW >50 kDaPoroshell 300SB-C18

2.1 x 75 mm, 5 µm660750-902

MW <25 kDaZORBAX 300Extend-C18

2.1 x 150 mm, 3.5 µm763750-902

Reversed-Phase LC/MS MethodsLC/MS of proteins and peptides is used to provide information for protein characterization, to accurately identify post-translational modifications of proteins, and to determine the molecular weight of synthetic and natural peptides. LC/MS is also used to provide protein identification in 2-D separations for proteomics applications. Therefore, LC/MS of proteins and peptides is a critical separation area, which requires some special column and mobile phaserecommendations. In general, smaller column sizes are used for LC/MS and TFA is generally not used in mobile phase because of reduced sensitivity in theMS with this mobile phase additive.

Initial Column Choices for LC/MS Separations of Proteins and Polypeptides

Low pH Mid and High pH

Capillary columns are used for high sensitivity protein and peptide applications. The 0.5 mm id columns are used for protein and protein digest separations while the 0.3 mm id columns are most often used for protein digests. These can be analyzed at high pH with an ammoniumhydroxide mobile phase. Nano columns (0.1 and 0.075 mm id) are often used in 2-D LC/MS systems for proteomics and the initial choice is C18 bonded phase.

Analytical LC/MS applications – 2.1 mm id columns provide good sensitivity when sample size is not limited. With Poroshell columns, smaller 1 mm column ids are used.

MW <50 kDaZORBAX 300SB-C8

2.1 x 150 mm, 3.5 µm863750-906

MW <1000 kDaPoroshell 300SB-C18

1.0 x 75 mm, 5 µm661750-902

MW <25 kDaZORBAX 300Extend-C18

2.1 x 150 mm, 3.5 µm763750-902

High Sensitivity/Proteomics Applications



Bio Ion-Exchange Column Methods

Bio MAb Monoclonal AntibodiesCation-Exchange (SCX, WCX)

Monoclonal Antibodies, Proteins,Peptides, and Glycoproteins

Recommended Initial Conditions

Mobile Phase: A: 20 mM sodium phosphate, pH 5.5

B: Buffer A plus 400 mM NaCl


Sample Size: 2 mg/mL; 5 µL injection


Detection: UV 220 nm

Mobile Phase: A: 20 mM sodiumphosphate, pH 5.0for WCX or pH 6.0for SCX


Gradient: 1-100% B in 30 min for 50 mm columns; 60 min for 250 mmcolumns



Detection: UV 220/280 nm

Mobile Phase: A: 10 mM Tris buffer,pH 8 for WAX or pH 9.0 for SAX


Gradient: 1-100% B in 30 min for 50 mm columns and 60 min for 250 mm columns



Detection: UV 220/280 nm

Anion-Exchange (SAX, WAX)Oligonucleotides, Proteins

Select Flow Rate Based on Column Diameter and Particle Size

2.1 mm id Columns 4.6 mm id Columns

Particle Size, µm Flow Rate, mL/min Particle Size, µm Flow Rate, mL/min5 0.1-0.5 1.7 0.1-0.3

1.7 0.1-0.8 3 0.1-0.55 0.1-0.8

10 0.1-1.0

448


Optimize ConditionsSome separations may require a specific buffer, ionic strength, pH, and/or temperature

Ionic Strength:

Selection of Buffers and pH:

Buffers play a key role in the optimization of separations. Phosphate buffers are typicallyused for antibodies and many biomolecules. The following are also recommended: MES,Tris, and ACES buffers. Use buffers of pH 5.0-6.5. pH can be adjusted usually by +/- 0.2units. For some specific proteins, buffers with higher pH (>pH 6.5) may be needed.Phosphoric acid, acetic acid, HCl and NaOH can be used to adjust pH.

pH gradients can also be used for elution.

Selection of Buffers and pH:

For anion-exchange, acetate and phosphatebuffers of pH 8.0-9.0 are recommended. pH canbe adjusted usually by +/- 0.2 units. For somespecific proteins, buffers with higher or lowerpH may be needed. Phosphoric acid, aceticacid, HCl and NaOH can be used to adjust pH.

pH gradients can also be used for elution.

Additives

Organic Solvents:

Acetonitrile, ethanol, methanol, and other similar solvents can be used up to 50%.

Detergents:

Non-ionic, anionic, and zwitterionic detergents can be used. Cationic detergents are not recommended.

Additives

Organic Solvents:

Acetonitrile, ethanol, methanol, and othersimilar solvents can be used up to 50%.

Detergents:

Non-ionic, cationic, and zwitterionicdetergents can be used. Anionic detergentsare not recommended.

Temperature:

Agilent Bio MAb and IEX columns are stable up to 80 °C. However, many proteins and biomolecules are heat labile. Be sure to establish thetemperature stability of your sample before routinely using high temperature for separation.

Certain ionic strength is required to sustain the function of columns. Usually, a minimal concentration of 10-20 mM salt is required. However,greater than 20 mM strength may prevent the adsorption of biomolecules onto the column. Commonly used salts are sodium and potassiumchloride and acetate. For elution, a typical salt concentration is 400-500 mM.

Note: Never use water alone for washing columns as it causes a significant increase in backpressure.



SEC Column Methods

Choose Initial Columns and Conditions for Size-Based Separation of Biomolecules, Aggregation Analysis – Peptides, Polypeptides, and Proteins

Peptides, Polypeptides, ProteinsMW >0.1-1,250 kDa

Select Column Based on Molecular Weight Range and Pore Size

Peptides, Polypeptides, ProteinsMW >0.1-10,000 kDa

Recommended Initial Separation Conditions

Column:

Mobile Phase:

Gradient:

Temperature:

Flow Rate:

Agilent Bio SEC (3 µm and 5 µm)

150 mM phosphate buffer, pH 7.0*

Isocratic in 30-60 min range

Recommended: 10-30 °C, Maximum: 80 °C

0.1-0.4 mL/min for 4.6 mm id columns0.1-1.25 mL/min for 7.8 mm id columns

Sample Size: ≤ 5% of total column volume

*Other aqueous buffers with high and low salt can be used

For additional information, see application note: Defining the Optimum Parameters for Efficient Size Separations of Proteins(publication # 5990-8895EN)

Agilent Bio SEC-3 (3 µm)

Pore Size MW range, kDa100Å 0.1-100150Å 0.5-150300Å 5-1,250

Agilent Bio SEC-5 (5 µm)

Pore Size MW range, kDa100Å 0.1-100150Å 0.5-150300Å 5-1,250500Å 15-5,0001000Å 50-7,5002000Å >10,000


450


After the initial chromatogram, additional changes may be needed to improve the separation, maintain protein solubility, or to decrease sampleinteraction with the chromatographic media. The ionic strength of the mobile phase can be adjusted up or down in strength to attain an optimizedseparation. pH can also be adjusted usually + 0.2 units. If further optimization is necessary, the upward or downward range should be expanded. A change of temperature or addition of an organic solvent can also be used.

For protocols requiring additional salt, these buffers are typical:

100-150 mM sodium chloride in 50 mM sodium phosphate, pH 7.0

100-150 mM sodium sulfate in 50 mM sodium phosphate, pH 7.0

50-100 mM urea in 50 mM sodium phosphate, pH 7.0

Other similar salts (e.g. KCl) and guanidine hydrochloride can also be used

pH Range:

2.0-8.5

5-10% ethanol (or other similar solvents) in 50 mM sodium phosphate, pH 7.0

5% DMSO in 50 mM sodium phosphate, pH 7.0

Temperature:

Typically, SEC separations are run at 20-30 °C. Separation of proteins and peptides may require higher temperature to improve both resolutionand recovery of proteins and hydrophobic peptides.

Maximum temperature of Bio SEC columns is 80 °C

Potential organic solvent additions include:



High Sensitivity Capillary Column Methods

Mobile Phase Considerations

Low pH

TFA is generally not used for LC/MS separations of proteins andpeptides. The first step is normally to replace TFA with 0.1 to 1%formic acid. Acetic acid, up to 1% can also be used as an alternativemobile phase modifier. At low pH, the best separation may still beobtained with TFA in the mobile phase. In some cases, the TFA can bedisplaced post-column with an alternative acid, such as propionic acid.

Mid and High pH

LC/MS can also be done at high pH with 10-20 mM NH4OH as amobile phase additive.

452


Capillary and Nano Columns• Highest sensitivity for your smallest sample sizes• Compatible with all LC/MS interfaces• Internal diameters of 0.5, 0.3, 0.1, and 0.075 mm• Packings/phases for both small and large molecules (80Å and 300Å pore sizes, respectively)• Ideal for 1-D and 2-D (proteomics) applications

Agilent ZORBAX Capillary (0.5 and 0.3 mm id) and Nano (0.1 and 0.075 mm id) columns are now availablein a wide variety of phases, pore sizes, and dimensions. These columns are ideal for very sample-limitedapplications because they provide enhanced sensitivity by reducing on-column sample dilution. This highsensitivity can be provided with exceptional reproducibility using Agilent columns and low dispersion HPLC instruments. The fastest growing application for capillary and nano columns is 2-D LC/MS forcomplex proteomics samples. Agilent provides all the columns needed for the 2-D separation – the SCXcolumns for the first dimension, the reversed-phase trapping column, and the reversed-phase column for the second dimension.

TIPS & TOOLS

Agilent offers a variety of e-Seminars andon-site training to help you learn how tobe a more effective chromatographer.

For more information, visitwww.agilent.com/chem/education

Nano Columns



ZORBAX Nano columns for highsensitivity protein digest analysisby LC/MSColumn: ZORBAX 300SB-C18

5065-99110.075 x 150 mm, 3.5 µm

Mobile Phase: A: Water + 0.1% Formic acid,B: ACN + 0.1% Formic acid

Flow Rate: 600 nL/min

Gradient: 2% B to 52% B in 25 min

Detector: Positive Ion Nano Electrospray MS

Sample: 100 fm (1 µL) Digest of 8 Proteins

LCSB008Time (min)

Intens.

2.5 5.0 7.5 10.0 12.5 15.0 17.5 20.0 22.5

0.5

1.5

1.0

A ZORBAX Nano HPLC column, 0.075 mm id, is used for high sensitivity LC/MS analysis of a protein digest sample.

High sensitivity with capillary columnsColumn: ZORBAX SB-C18

5064-82550.3 x 150 mm, 5 µm

Column: ZORBAX SB-C185064-82560.5 x 150 mm, 5 µm

Column: ZORBAX SB-C18863600-9021.0 x 150 mm, 3.5 µm

Column: ZORBAX SB-C18883975-9024.6 x 150 mm, 5 µm

Sample: 200 ng Biphenyl

LCCN002

Time (min)

mAU

0.3 mm

0.5 mm

1.0 mm

0 2.5 5.0 7.5 10.0 12.5 15.0 17.5

0

400

300

200

600

800

1000

1200

1400

4.6 mm

Sample-limited applications require capillary column dimensions to minimize on-column sample dilution and to enhance sensitivity. The 0.3 mm capillary in this example provides100 times more sensitivity than the standard 4.6 mm column. Agilent Nanobore (0.1 mm to 0.075 mm id) columns can provide up to 2,000 times more sensitivity for your mostlimited sample applications.

454


LCBP014

020 25 30 35 40 45 50 55

1

2

3

x107

Intens.

Time (min)

Peptide phosphorylation sites LC andLC/MS using Capillary LC columnsColumn: ZORBAX 300SB-C18

5064-82680.5 x 150 mm, 3.5 µm

Mobile Phase: A: Water + 0.1% Formic acidB: Acetonitrile + 0.1% Formic acid

Flow Rate: 5.5 µL/min

Gradient: 5-55% B in 50 min, to85% B from 55-57 min


MS Conditions: LC/MS: Pos. Ion ESI with LC/MSD trap

Vcap: 4000 VDrying gas flow: 7 L/min Drying gas temperature: 250 °CNebulizer: 15 psiCapillary Exit Volt: 50 V MaxAccum Time: 300 msTotal Averages: 3 Isolation Width: 3 m/zFrag Ampitude: 1.0 V

Sample: Beta case in digest, 100 nL (4 pmol)

LCBP037Time (min)

UV

at 2

06 n

m

UV

20

40

60

80

100

10 15 20 25 30 35 40 45 50

0

Time (min)

% R

elat

ive

Abun

danc

e

MS Full Scan MS

phosphopeptide

343.0559.5

688.4

1032.0

1275.4 1582.0

747.3

982.5 1022.9

1106.71490.8

1690.0

[MH2-H20]2+[MH2-H2PO4]2+

0.2

0.4

0.6

0.8

x107

10 15 20 25 30 35 40 45 50

0.0m/z

% R

elat

ive

Abun

danc

e

0.5

1.0

1.5

2.0

2.5x105

400 800 160016000.0

MS/MS of [M+2H] 2+ at m/z 1032

m/z

% R

elat

ive

Abun

danc

e

0.5

1.0

1.5

2.0

2.5x104

400 800 160016000.0

Sample Preparation of Human Serum:Major serum proteins removed using Multiple Affinity Removal Column:4.6 x 100 mm, P/N 5185-5985Followed by 1-D gel digest

Base Peak Chromatogram

Human serum: Low abundance protein isolationand identification from 1-D gel band by LC/MSColumn: ZORBAX 300SB-C18

Trap: 0.3 x 5 mm, 5 µm, 5065-9913Analytical: 0.3 x 150 mm, 5 µm, 5064-8263

Mobile Phase: A: Water + 0.1% Formic acidB: Acetonitrile + 0.1% Formic acid


Gradient: 0 min 3% B5 min 3% B (loading)50 min 45% B52 min 80% B57 min 80% B60 min 3% B

Sample: Band from 1-D in gel digest

Proteins Identified1. a-1-Antichymotrypsin

2. Antithrombin-III Precursor

3. Complement Factor B Precursor



Capillary columns for HPLC analyses with UV and MS detectionColumn: ZORBAX 300SB-C18

5064-82630.3 x 150 mm, 5 µm

Mobile Phase: 5-55% B in 50 min, to 85% B from 55-57 minA: Water + 0.1% Formic acidB: Acetonitrile + 0.1% Formic acid

Flow Rate: 5.5 µL/min


MS Conditions: LC/MS: Pos. Ion ESI withLC/MSD trap-Vcap 4000 V

Drying Gas Flow: 7 L/minDrying Gas Temperature: 250 °CNebulizer: 15 psiCapillary Exit Volt: 50 VMax Accum Time: 300 msTotal Averages: 3Isolation Width: 3 m/zFrag Ampitude: 1.0 V

Sample: 100 nLBeta Casein Digest (4 pmol)

LCSB007

Time (min)

UV

at 2

06 n

m

UV

20 25 30 35 40 45 5015100

20

40

60

80

100

Time (min)

% R

elat

ive

Abun

danc

eMS

20 25 30 35 40 45 5015100.0

0.2

0.4

0.6

0.8

x10

A ZORBAX 300SB-C18 capillary column (0.3 mm id) is used for the separation of the protein digest. Detection is by both UV andElectrospray MS. MS detection can be used for identification ofpeptide fragments.

456


2-D LC/MS Analyses Using ZORBAX Capillaryand Nano LC Columns

Typical Column Configuration for 2-D HPLC

Flow path of an Agilent customized Nanoflow Proteomics Solution system.1. Sample loading, elution from SCX and trapping on enrichment column2. Valve switch in column compartment, elution from enrichment column; separation on RP, and MS anaylsis

1100/1200 Series quaternary pump

1100/1200 Series micro well plateautosampler

Waste

Reversed-phase enrichment column

Nanopump

SCX Strong cation-exchange column

Reversed-phase column 1100/1200 Series columncompartment

Detection (1100/1200 Series LC/MSD Trap)

1100/1200 Series quaternary pump

1100/1200 Series micro well plateautosampler

Waste

Reversed-phase enrichment column

Nanopump

SCX Strong cation-exchange column

Reversed-phase column 1100/1200 Series columncompartment

Detection (1100/1200 Series LC/MSD Trap)



Proteins in a complex sample by 2-D HPLC with Nano HPLC columnsColumn: ZORBAX 300SB-C18

5065-99130.3 x 5 mm, 5 µm

Column: ZORBAX 300SB-C185065-99110.075 x 150 mm, 3.5 µm

Mobile Phase: Quaternary Pump: 3% Acetonitrile/0.1% Formic acidNanopump: A = Water, 0.1% Formic acid, B = ACN,0.1% Formic acid

Flow Rate: Quaternary Pump: 30 µL/minNanopump: 300 nL/min

Gradient: Quaternary Pump: IsocraticNanopump:6 min = 3% B, 120 min = 60% B, 125 min = 80% B,130 min = 80% B, 131 min = 3% B, 140 min = 3% B

MS Conditions: Source: Nano ESI, drying gas flow: 5 L/min, drying gas temp: 225 °CIon Trap: Skim: 1:35 V, cap exit offset: 115 V, octupole 1:12 V,octupole 2:3.5 V, trap drive: 80 V. ICC: on, averages: 4, max accutime: 150 ms; target 60.000, ion mode positive, MS/MS mode.

Sample: Tryptic Digest of bovine serum albuminVolume: 1 to 8 µLSalt Step Elution: 8 mL of 10 mM-100 mM KCI (10 mM increments),125 mM, 150 mM, 200 mM, 300 mM, 500 mM, 1 M.

LCCN004

Time (min)

Intens.

30 mM KCI

60 mM KCI

75 mM KCI

120 mM KCI

5 10 15 20 25 30 35 40

0.5

1.0x106

0.5

1.0x106

4

2

6

x105

4

2

6x105

Tryptic digest of bovine serum albumin (BSA).The base peak chromatograms show aselection of fractions from a 2-D HPLCseparation. Single chromatograms representpeptides from BSA eluting at a given saltconcentration followed by enrichment andreversed-phase chromatography.

458


ZORBAX Bio-SCX Series IIZORBAX has Bio-SCX Series II columns designed for optimized 2-D separations of peptides and proteins using LC/MS. This packing is based on ultra-pure 3.5 µm ZORBAX silica particles, bonded with a bio-friendly polymer that is functionalized with sulfonic acid groups. This gives strong retention and good peak shape in the ion-exchange step of 2-D analysis of peptides and proteins.



SurfaceArea

pH Range Functionality

MaxPressure

ZORBAX Bio-SCX Series II 300Å 90 m2/g 2.5-8.5 Sulfonic acid 350 bar

ZORBAX Bio-SCX Series II

Description Size (mm) Particle Size (µm)Bio-SCXSeries II

Capillary 0.3 x 35 3.5 5065-9912Capillary 0.8 x 50 3.5 5065-9942

Nano Columns



ZORBAX Bio-SCX Series II provides more retention of small peptidesColumn: ZORBAX Bio SCX Series II

5065-99120.3 x 35 mm, 3.5 µm

Mobile Phase: 95% 40 mM NaCl: 5% ACN,0.3% Formic acid


Detector: 230 nm

Sample: Synthetic Dipeptides

LCIE002

Time (min)

mAU

420 6 8 10

12

02040

Time (min)

mAU

420 6 8 10

12

02040

The new ZORBAX Bio-SCX Series II column retains smaller peptides more strongly than some other SCX columns. The result is increased resolution of more hydrophilic peptidesfragments and more accurate identification when these columns are used in 2-D HPLC analysis.

1. Trp - Tyr2. Mct - Trp

460


ZORBAX HPLC Capillary Columns (glass-lined stainless steel)

Description Size (mm) Particle Size (µm) 300SB-C18 300SB-C8Poroshell300SB-C8 300Extend-C18

Bio-SCXSeries II

Capillary 0.8 x 50 3.5 5065-9942Capillary 0.5 x 250 5 5064-8266Capillary 0.5 x 150 5 5064-8264Capillary RR 0.5 x 150 3.5 5064-8268Capillary 0.5 x 75 5 5065-4468Capillary 0.5 x 35 5 5064-8294Capillary RR 0.5 x 35 3.5 5065-4459Capillary 0.3 x 250 5 5064-8265Capillary 0.3 x 150 5 5064-8263Capillary 0.3 x 35 5 5064-8295Capillary 0.3 x 35 3.5 5065-9912Capillary RR 0.3 x 150 3.5 5064-8267 5065-4460 5065-4464Capillary RR 0.3 x 100 3.5 5064-8259 5065-4461 5065-4465Capillary RR 0.3 x 75 3.5 5064-8270 5065-4462 5065-4466Capillary RR 0.3 x 50 3.5 5064-8300 5065-4463 5065-4467Replacement Screens, 10/pk 5065-4427 5065-4427 5065-4427 5065-4427

ZORBAX Nano HPLC Columns (PEEK)


(µm)300SB-C18USP L1

300SB-C8USP L7

Nano RR 0.1 x 150 3.5 5065-9910Nano RR 0.075 x 150 3.5 5065-9911Nano RR 0.075 x 50 3.5 5065-9924 5065-9923Trap/Guard, 5/pk 0.3 x 5 5 5065-9913 5065-9914Trap/Guard Hardware kit 5065-9915 5065-9915

ZORBAX 300SB-C18 trap/guard, 5065-9913



MicroBore (1.0 mm id) Columns• High sensitivity for small sample sizes• Compatible with LC/MS interfaces• Wide variety of bonded phases• Silica and polymeric particles

Agilent MicroBore (1.0 mm id) columns are a good choice when sample sizes are limited. They can improvedetection limits 5 times over 2.1 mm id columns when the same sample mass is used. This increase insensitivity can be critical. MicroBore columns use low flow rates (typically ~ 50 µL/min). Therefore, thesecolumns are ideal for use with detectors requiring low flow rates such as some mass spectrometers andwith capillary LC systems.

Optimum performance is achieved when MicroBore columns are used with UHPLC/HPLC Microboresystems. A wide variety of bonded phases is available for use up to 400 bar including StableBond, 300SB-C18, 300SB-C8, and Poroshell columns. Polymeric reversed-phase, PLRP-S, and ion-exchange PL-SAX and PL-SCX are also available for applications requiring exceptionally stable wide pore particles.Guard columns are also now available with an adjustable tube stop depth to provide a perfect zero deadvolume connection every time.

Separation of a tryptic digest onZORBAX MicroBore 300SB-C18Column: ZORBAX 300SB-C18

863630-9021.0 x 150 mm, 3.5 µm

Mobile Phase: Gradient: 2-60% B in 60 minA: 0.1% TFAB: 0.075% TFA/80% ACN


Temperature: 50 °C


Sample: 2 µLTryptic Digest of rhGH

LCMB001Time (min)

20 30 40 5010 25 35 45 55150 5This example of a tryptic digest separated on aMicroBore column demonstrates the high sensitivityand resolution possible with 1.0 mm id columns.

Sterically Protected 300StableBond Bonded Phase

462


Peptide separation on Agilent PLRP-S 100Å 5 µm columns

21

3

4

ABC

min0 8

Standard curve data-point graphs on Agilent PLRP-S columns

30

0

10

20

40

50

60

70

80

90

50 100 1500 50 100 1500

100

0

20

40

60

80

120

40

0

20

60

80

100

120

140

160

50 100 1500 50 100 1500

80

0

40

50

60

70

90

30

20

10

Insulin Oxytocin Angiotensin II Angiotensin I

Peak

Are

a

Peak

Are

a

Peak

Are

a

Peak

Are

a

Microbore HPLC for sensitive peptide analysisColumn: PLRP-S 100Å 5 µm, 150 mm x various idMobile Phase: A: 0.01 M Tris HCI, pH 8

B: A + 0.35 M NaCl, pH 8

Flow Rate: 1 mL/min

Gradient: Linear 20% ACN, 0.1% TFA to 50% ACN, 0.1% TFAover 15 min

Injection Volume: 0.5 µL

Sample Conc: 0.25 mg/mL


1. Oxytocin2. Angiotensin II3. Angiotensin I4. Insulin

conc (ng) conc (ng) conc (ng) conc (ng)

Peak IdentificationA. 1.0 mm id (flow rate 47 µL/min)B. 2.1 mm id (flow rate 200 µL/min)C. 4.6 mm id (flow rate 1 mL/min)

Peak Identification1.0 mm2.1 mm4.6 mm



MicroBore (1.0 mm id)



300SB-C8USP L7

MicroBore 1.0 x 250 5 861630-902MicroBore RR 1.0 x 150 3.5 863630-902 863630-906MicroBore RR 1.0 x 50 3.5 865630-902 865630-906MicroBore Guard, 3/pk 1.0 x 17 5 5185-5920 5185-5920


(µm)Poroshell300SB-C18

Poroshell300SB-C8

Poroshell300SB-C3

Poroshell300Extend-C18

MicroBore 1.0 x 75 5 661750-902 661750-906 661750-909 671750-902MicroBore Guard, 3/pk 1.0 x 17 5 5185-5968 5185-5968 5185-5968


(µm)

PLRP-S100ÅUSP L21

PLRP-S300ÅUSP L21

PLRP-S1000ÅUSP L21

PLRP-S4000ÅUSP L21

MicroBore 1.0 x 150 3 PL1312-3300MicroBore 1.0 x 50 3 PL1312-1300 PL1312-1301MicroBore 1.0 x 50 5 PL1312-1500 PL1312-1501 PL1312-1502 PL1312-1503MicroBore 1.0 x 50 8 PL1312-1802 PL1312-1803


(µm)PL-SCX1000Å

PL-SCX4000Å

PL-SCX1000Å

PL-SCX4000Å

MicroBore 1.0 x 50 5 PL1351-1502 PL1351-1503 PL1345-1502 PL1345-1503

464


Purification – Prep HPLCAgilent has a comprehensive range of silica and polymeric HPLC columns and media designed forbiomolecule purification. There are high efficiency small particle prep columns optimized for the purificationof µg and mg amounts of a biopharmaceutical drug candidate and fully porous bulk media, to packdevelopment and process columns to purify multiple 100 g, kg and multi-kg of API.

Some columns are specifically designed to address the needs of high efficiency purification, while other products provide easy scale-up from small particle analytical columns to full scale API production. Table 1 shows prep column/media options and the quantity of product that can be purified.

BioPharmaceutical Lifecycle Discoveryµg mg

high efficiency

Developmentg

Productionkg multi-kg

high throughput

Reversed-Phase

Ion-Exchange

Size Exclusion

mRP-C18

ZORBAX Prep HT300Å StableBond

VariTide RPC

PLRP-S 100Å, 300Å,1000Å, 4000Å

PL-SAX

PL-SCX

ZORBAX GF-250/450

Polymeric Prep HPLC Columns

Table 1: Agilent columns and media for biomolecule purification – chromatographic type, product family and purification scale.



TIPS & TOOLS

Purification Column Selection

Application Technique Notes Agilent ColumnsProteomics Reversed-Phase A specialist high recovery column for proteomics applications. It is designed for µg scale

purifications with maximum recovery.mRP-C18

All Biomolecules Reversed-Phase High efficiency 300Å silica-based particles. ZORBAX PrepHT 300SBSynthetic Peptides Reversed-Phase Polymeric material designed for the purification of synthetic peptides. It is a high efficiency

single-column solution for the full range of synthetic peptides, acidic, basic, hydrophobicand hydrophilic, and covers the size range of peptides produced by both solution and solidphase synthesis.

VariTide RPC

All Biomolecules Reversed-Phase The premium polymeric reversed-phase family with a range of pore sizes and particle sizesto enable high efficiency laboratory scale purification using small particle prep column,and scale-up to high yield production purification with larger particles at the processscale. Use PLRP-S when purification will be scaled up to produce APIs and will needregulatory documentation.

PLRP-S

ü 3 µm and 5 µm for high efficiencyü 8 µm, 10 µm, 10-15 µm, 15-20 µm, 30 µm and 50 µm particles for larger scale

and low pressure purificationAll Biomolecules Ion-Exchange A fully porous strong anion-exchanger PL-SAX

ü 5 µm particle size for high efficiency separationsü 8 µm, 10 µm and 30 µm particles for larger scale medium and low pressure purificationA fully porous strong cation-exchanger PL-SCXü 5 µm particle size for high efficiency separationsü 8 µm, 10 µm and 30 µm particles for larger scale medium and low pressure purification

Further information can be found inthe following publication:

Biomolecule Purification(publication # 5990-8335EN)


466


ZORBAX PrepHTHigh purity, high recovery, and high throughput can be easily achieved with Agilent ZORBAX PrepHTcolumns. These are available in a variety of bonded phases – StableBond 300Å, C18, C8, C3, and CN – for optimized resolution and loadability under any conditions.

ZORBAX PrepHT columns are packed with 5 and 7 µm particle sizes for very high resolution. The high resolution allows high loadability, high yield, and high purity of compounds. The larger diameter columns and mechanically stronger ZORBAX particles allow for flow rates up to 100 mL/min, thus increasing throughput.

ZORBAX PrepHT columns are designed for rapid scale-up from analytical to preparative scale without losingresolution. For complex separations on larger columns (21.2 mm id, 150 mm length and longer), Agilent hascarefully chosen the 7 µm particle size to achieve a balance between high efficiency and high loadability.


Hardware DescriptionSize

(mm)Particle Size


300SB-C8USP L7

300SB-CNUSP L10

300SB-C3USP L56

PrepHT Cartridge Columns (require endfittings kit 820400-901)PrepHT Cartridge 21.2 x 250 7 897250-102 897250-106 897250-105 897250-109PrepHT Cartridge 21.2 x 150 7 897150-102 897150-106 897150-109PrepHT Cartridge 21.2 x 150 5 895150-902 895150-906 895150-909PrepHT Cartridge 21.2 x 100 5 895100-902 895100-906 895100-909PrepHT Cartridge 21.2 x 50 5 895050-902 895050-906 895050-909PrepHT Endfittings, 2/pk 820400-901 820400-901 820400-901 820400-901PrepHT Guard Cartridge, 2/pk 17.0 x 7.5 5 820212-921 820212-918 820212-924 820212-924Guard Cartridge Hardware 820444-901 820444-901 820444-901 820444-901

ZORBAX 300Å StableBond Prep HT Cartridge Columns



PLRP-S for Prep to Process• Discovery stage to multi-kg cGMP production reduces method development time• Chemical stability for separations, optimization, sanitation, and regeneration increases selectivity

and column lifetime• Single batch packing of multiple columns reduces system downtime and validation costs

The PLRP-S media, rigid poly(styrene/divinylbenzene) particles, are available in a range of pore sizes forsmall molecule, synthetic biomolecule and macromolecule purification. Their thermal and chemical stabilitymakes them ideal for purifications that require extreme conditions for sample preparation, compoundelution, and column regeneration.

Capacity and resolution are two key parameters for maximizing the throughput of a purification. With a widechoice of pore sizes and extended range of operating conditions, PLRP-S provides more options to achievethe optimum process. Particle sizes range from 3 µm to 50 µm for scale-up from the µg/mg discovery stageto multi-kg cGMP production. Excellent chemical stability, up to 1 M NaOH, permits sanitation andregeneration that increase column lifetime. PLRP-S media batch sizes of up to 600 L are available, providingsingle batch packing of multiple columns.

As part of our commitment to quality and continuity of supply, all manufacturing is carried out under a fullydocumented process. A Type II Drug Master File and regulatory support files are available for processmaterials, and facility audits are routinely conducted.

468


PLRP-S Prep to Process Application Guide

ApplicationPLRP-S Media Pore Size

100Å 300Å 1000Å 4000ÅSynthetic biomolecules, peptides, and oligonucleotides 3 3

Recombinant biomolecules, peptides, and proteins 3 3

Large biomolecules, antibodies, DNA fragments 3 3

Small molecules, unstable compounds including metal sensitivity 3



3 µm: 4000 psi (300 bar)



Purification of a 25-mer trityl-off oligonucleotideand analytical quantitation of the fraction using PLRP-S 100Å, 4.6 x 50 mm

0

0

80

min 12.5VLC0053

0

0

200

min

mV

mV

25

Purity (CE): 90.54%

Recovery: 83.20%

Crude bradykinin prep loadColumn: PLRP-S 100Å

PL1512-51004.6 x 250 mm, 10 µm

Sample: 30 µL containing 1.5 mg of crude peptide

Mobile Phase: 0.1% TFA in 21% ACN:79% water

Flow Rate: 1 mL/min (360 cm/hr)0 30min

VLCbradykinin

% Purity (Bradykinin)% Purity (Impurity)

Fraction analysis –the concentrationoverload purification

HPLC Purity %

Fraction number

100

0

HPLC analysis of the fractions collected across thepeak showed that fractions 1 to 4 contained only the peptide of interest and that the level of the criticalimpurity increased with increasing fraction number.Using the high efficiency PLRP-S column it waspossible to obtain from the crude, 91.7% pure, a recovery of 97% with 100% purity. For moreinformation, see application note 5990-7736EN.

% H

PLC

Purit

y

Column: PLRP-S 100ÅPL1512-13004.6 x 50 mm, 3 µm

Mobile Phase: A: 100 mM Triethylammonium acetate (TEAA)B: 100 mM TEAA in 25:75 Acetonitrile:water

Flow Rate: 1 mL/min

Gradient: 25% B 0 min, 35% B 2 min, 45% B 22.5 min, 45% B 23 min, 25% B 23.05 min, 25% B 26 min

Temperature: 80 ºC

470


Prep to Process PLRP-S

Size (mm) Particle Size (µm)PLRP-S100Å

PLRP-S300Å

PLRP-S1000Å

PLRP-S4000Å

100 x 300 30 PL1812-3102 PL1812-3103100 x 300 15-20 PL1812-6200 PL1812-6201100 x 300 10-15 PL1812-6400 PL1812-6401100 x 300 10 PL1812-6100 PL1812-6101100 x 300 8 PL1812-6800 PL1812-680150 x 300 8 PL1712-6800 PL1712-680150 x 150 30 PL1712-3702 PL1712-370350 x 150 15-20 PL1712-3200 PL1712-320150 x 150 10-15 PL1712-3400 PL1712-340150 x 150 10 PL1712-3100 PL1712-3101 PL1712-3102 PL1712-310350 x 150 8 PL1712-3800 PL1712-380125 x 300 15-20 PL1212-6200 PL1212-620125 x 300 10-15 PL1212-6400 PL1212-640125 x 300 10 PL1212-6100 PL1212-610125 x 300 8 PL1212-6800 PL1212-680125 x 150 30 PL1212-3702 PL1212-370325 x 150 10 PL1212-3100 PL1212-3101 PL1712-3102 PL1712-310325 x 150 8 PL1212-3800 PL1212-380125 x 50 10 PL1212-1102 PL1212-1103PLRP-S Method Development Columns4.6 x 250 30 PL1512-5702 PL1512-57034.6 x 250 15-20 PL1512-5200 PL1512-52014.6 x 250 10-15 PL1512-5400 PL1512-54014.6 x 250 10 PL1512-5100 PL1512-5101 PL1512-5102 PL1512-51034.6 x 250 8 PL1512-5800 PL1512-58014.6 x 150 30 PL1512-3702 PL1512-37034.6 x 150 15-20 PL1512-3200 PL1512-32014.6 x 150 10-15 PL1512-34014.6 x 150 10 PL1512-3100 PL1512-3101 PL1512-3102 PL1512-31034.6 x 150 8 PL1512-3800 PL1512-3801



PLRP-S Bulk Media

Particle Size (µm) UnitPLRP-S100Å

PLRP-S300Å

PLRP-S1000Å

PLRP-S4000Å

50 1 kg PL1412-6K00 PL1412-6K01 PL1412-6K02100 g PL1412-4K00 PL1412-4K01 PL1412-4K02

30 1 kg PL1412-6702 PL1412-6703100 g PL1412-4702 PL1412-4703

15-20 1 kg PL1412-6200 PL1412-6201100 g PL1412-4200 PL1412-4201

10-15 1 kg PL1412-6400 PL1412-6401100 g PL1412-4400 PL1412-4401

10 1 kg PL1412-6100 PL1412-6101 PL1412-6102 PL1412-6103100 g PL1412-4100 PL1412-4101 PL1412-4102 PL1412-4103

8 1 kg PL1412-6800 PL1412-6801For larger quantities, please contact your local Agilent sales office

472


PL-SAX and PL-SCX for Prep to Process• Ion-exchange purifications over a wider pH range extend applications• HPLC flow rates and rapid equilibration reduce purification cycle times• Large pore size for improved mass transfer delivers high speed, high resolution purifications

These rigid, strong ion-exchange materials are extremely hydrophilic and are designed for purification ofbiomolecules. The PL-SAX and PL-SCX materials are totally polymeric and are chemically and thermallystable over a full range of HPLC conditions. The strong ion-exchange functionalities, covalently linked to achemically stable polymer, facilitate ion-exchange purifications over a wider pH range. This stability can beexploited for column sanitation and clean-up. Thermal stability also enables the use of denaturing conditionsand stabilizing/solubilizing agents for the purification of target compounds, as encountered in thepurification of synthetic oligonucleotides with self-complementary sequences.

Both the 1000Å and 4000Å wide-pore materials are mechanically stable and robust and can be operatedover a wide range of linear velocities, with fast loading of dilute solutions and wash cycles. HPLC flow ratesand rapid equilibration reduces purification cycle times.

Packing in dynamic axial compression (DAC) column hardware is straightforward and high efficiencycolumns are achieved with excellent reproducibility and lifetimes. The 1000Å pore size is for high-capacitypurifications and the 4000Å gigaporous particles with improved mass transfer are intended for largebiomolecules and high-speed, high-resolution purifications.




PL-SAX PL-SCXMatrix Fully polymeric Fully polymericPore Sizes 1000Å, 4000Å 1000Å, 4000ÅParticle Sizes 10 µm, 30 µm 10 µm, 30 µmBead Form Rigid spherical Rigid sphericalFunctionality Quaternary amine Sulfonic acidPressure Stability 3000 psi 3000 psiTemperature Stability 80 °C 80 °CpH Range 1-14 1-14Eluent Compatibility All anion-exchange buffers All cation-exchange buffersPacked Bed Density 0.39 g/mL 0.39 g/mL

Purification of a large oligonucleotideColumn: PL-SAX 1000Å, 8 µmMobile Phase: A: 93% 0.1 M TEAA, pH 7:7% ACN

B: 93% 0.1 M TEAA, 3.24 M ammonium acetate, pH7:7% ACN



Temperature: 60 °C

Detector: UV, 290 nm 0

0

80

min

91-mer

35

%B

VLC0054

Preparative fractionation of a culture filtrate containing amyloglucosidases on Agilent PL-SAX 4000ÅColumn: PL-SAX

PL1551-18034.6 x 50 mm, 8 µm

Mobile Phase: A: 0.01 M Tris HCI, pH 8B: A + 0.5 M NaCl, pH 8




min0 30

Preparative fraction

474


Prep to Process PL-SAX and PL-SCX

Dimensions Particle Size (µm)PL-SAX 1000Å

PL-SAX4000Å

PL-SCX 1000Å

PL-SCX4000Å

100 x 300 30 PL1851-3102 PL1851-3103 PL1845-3102 PL1845-3103100 x 300 10 PL1851-2102 PL1851-2103 PL1845-2102 PL1845-210350 x 150 30 PL1751-3702 PL1751-3703 PL1745-3702 PL1745-370350 x 150 10 PL1751-3102 PL1751-3103 PL1745-3102 PL1745-310325 x 150 30 PL1251-3702 PL1251-3703 PL1245-3702 PL1245-370325 x 150 10 PL1251-3102 PL1251-3103 PL1245-3102 PL1245-310325 x 50 10 PL1251-1102 PL1251-1103 PL1245-1102 PL1245-11037.5 x 150 8 PL1151-3802 PL1151-38037.5 x 50 8 PL1151-1802 PL1151-1803 PL1145-1802 PL1145-1803PL-SAX and PL-SCX Method Development Columns4.6 x 250 30 PL1551-5702 PL1551-5703 PL1545-5702 PL1545-57034.6 x 250 10 PL1551-5102 PL1551-5103 PL1545-5102 PL1545-51034.6 x 150 30 PL1551-3702 PL1551-3703 PL1545-3702 PL1545-37034.6 x 150 10 PL1551-3102 PL1551-3103 PL1545-3102 PL1545-3103

PL-SAX and PL-SCX Bulk Media

Particle Size (µm) UnitPL-SAX1000Å

PL-SAX4000Å

PL-SCX1000Å

PL-SCX4000Å



For larger quantities, please contact your local Agilent sales office

Prep to Process PL-SAX and PL-SCX Columns and Bulk Media



Peptide PurificationVariTide is a cost-effective solution for the production of synthetic peptides. This column lets you managethe cost and efficiency of high-volume synthetic peptide purification, from µg to g scale. VariTide provides a solution for peptide houses that manufacture small quantities of hundreds or thousands of peptides wheremanufacturing time is the economic driving force.

VariTide RPC Columns for Synthetic Peptides• A single column to cover the full range of synthetic peptides• Small particle size for maximum efficiency, even with 1 and 2 in prep columns• Bulk media to pack 1 and 2 in prep columns for the purification of mg to g quantities

VariTide RPC columns and media are part of the VariPep Peptide Solution. This is the recommended optionfor cost-effective separation and purification of synthetic peptides using generic methods.

VariTide RPC Columns for Synthetic PeptidesSize (mm) Part No.21.2 x 250 PL1E12-5A0510.0 x 250 PL1012-5A054.6 x 250 PL1512-5A05

VariTide RPC Bulk MediaDescription Part No.100 g PL1412-4A051 kg PL1412-6A05

VariTide RPC Columns

476


Crude peptide screenColumn: VariTide RPC

PL1512-5A054.6 x 250

Mobile Phase: AcidicA: 0.1% TFA in 95% water: 5% ACNB: 0.1% TFA in 50% water: 50% ACNBasicA: 5% ACN, 95% 20 mm ammoniumcarbonate pH 9.5B: 50% ACN, 50% 20 mm ammoniumcarbonate pH 9.5

Flow Rate: 1.0 mL/min (360 cm/h)



0VLC0052

30min

Major impurity notseparated at acidic pH

Acidic

Basic

VariPure IPE• Pre-packed for convenience• Removal of ion-pairing agents for improved productivity• High performance and economy for excellent efficiency

VariPure IPE is a polymer-supported quaternary-amine resin with a bicarbonate counter ion, designed forremoving acidic ion-pair reagents, such as trifluoroacetic acid (TFA), formic acid or acetic acid. VariPure IPEis a high performance and economical acid removal material conveniently supplied as pre-packed SPE typedevices. The particle size, capacity and device geometry are matched to provide sufficient residence time toachieve effective ion-air extraction under gravity flow. For acid labile peptides, removal of the ion-pairingagent prevents acid degradation of the peptide during post-HPLC work-up, and increases the yield ofpurified product.

VariPure IPE

LoadingCounter-ionRemoval Capacity Unit Part No.

100 mg per 3 mL tube ~ 5 mL 0.1% TFA 50/pk PL3540-D603VP500 mg per 6 mL tube ~ 25 mL 0.1% TFA 50/pk PL3540-C603VP1 g per 20 mL tube ~ 50 mL 0.1% TFA 25/pk PL3540-P603VP25 g PL3549-3603VP



BioHPLC Columns LiteratureTitle Column/Product Application Publication Number Publication TypeRapid Analysis of Adenovirus Type 5 Particles with Bio-Monolith Anion-Exchange HPLC Columns to Supportthe Development of a High-Titre Manufacturing Platform

Bio-Monolith QA Adenovirus 5990-5524EN Application Note

Separation of Two Sulfurated Amino Acids with otherSeventeen Amino Acids by HPLC with Pre-ColumnDerivatization

Eclipse Plus-C18 Amino acid analysis 5990-5977EN Application Note

Rapid, Accurate, Sensitive, and Reproducible HPLCAnalysis of Amino Acids

ZORBAX Eclipse AAA Amino acid analysis 5980-1193EN Application Note

High-Speed Amino Acid Analysis (AAA) on 1.8 µmReversed-Phase (RP) Columns

ZORBAX Eclipse Plus Amino acid analysis 5989-6297EN Application Note

Improved Amino Acid Methods Using Agilent ZORBAX Eclipse Plus C18 Columns for a Varietyof Agilent LC Instrumentation and Separation Goals


Rapid and Precise Determination of Cellular Amino AcidFlux Rates using HPLC with Automated Derivatizationwith Absorbance Detection


Agilent PL-SAX 1000Å HPLC Columns and Media PL-SAX Analysis/Prep -Oligonucleotides

5990-8200EN Flyer

Compliance for Biopharmaceutical Laboratories LC columns Compliance 5990-7001EN PrimerMacroporous Reversed-Phase C18 High-RecoveryProtein Fractionation HPLC Column

mRP-C18 Human serum,Biomarkers

5989-2714EN Brochure

Rapid Human Polyclonal IgG Quantification using theAgilent Bio-Monolith Protein A HPLC Column

Bio-Monolith IgG 5989-9733EN Application Note

Rapid IgM Quantification in Cell Culture Production and Purification Process Monitoring using the Agilent Bio-Monolith QA Column

Bio-Monolith QA IgM 5989-9674EN Application Note

Optimization of Protein Separations on Weak Cation-Exchange Columns – a Study of the Particle Size,Buffer Salts and Gradients

Bio IEX MAbs 5990-8833EN Technical Poster

(Continued)

478


pH Gradient Elution for Improved Separation ofMonoclonal Antibody Charged Variants

Bio MAb MAbs 5990-9629EN Application Note

Characterization of Monoclonal Antibodies on the Agilent 1260 Infinity Bio-inert Quaternary LC by Size Exclusion Chromatography using the Agilent Bio SEC Columns

Bio SEC MAbs 5990-6414EN Application Note

Agilent BioHPLC Columns for the Characterization ofMonoclonal Antibodies

Biocolumns MAbs 5990-7753EN Flyer

Fast Separation of Monoclonal Antibody and Dimer bySEC with Agilent Bio SEC

Bio SEC MAbs 5990-8613EN Application Note

Choosing a ZORBAX Poroshell Phase (C3, C8, or C18) forFast Separation of Monoclonal Antibodies

Poroshell 300 MAbs 5989-0071EN Application Note

Determination of the Glycosylation Status of IntactRecombinant Human Antibodies using Time of FlightMass Spectrometry

Poroshell 300 MAbs N/A Technical Poster

High Speed and Ultra-High Speed Peptide Mapping ofHuman Monoclonal IgG on Poroshell 300SB-C18, C8,and C3


Rapid HPLC Analysis of Monoclonal Antibody IgG1 HeavyChains using ZORBAX Poroshell 300SB-C8


Comparison of ZORBAX StableBond 300Å LC Columns toOptimize Selectivity for Antibody Separations Using HPLCand LC/MS

ZORBAX 300SB MAbs 5989-6840EN Application Note

Ultra High Speed and High Resolution Separations ofReduced and Intact Monoclonal Antibodies with AgilentZORBAX RRHD Sub-2 µm 300 Diphenyl UHPLC Column

ZORBAX RRHD 300-Diphenyl MAbs 5990-9668EN Application Note

Reversed-Phase Optimization for Ultra Fast Profiling ofIntact and Reduced Monoclonal Antibodies using Agilent ZORBAX Rapid Resolution High Definition 300SB-C3 Column

ZORBAX RRHD 300SB-C3 MAbs 5990-9667EN Application Note

Title Column/Product Application Publication Number Publication Type

BioHPLC Columns Literature

(Continued)



BioHPLC Columns LiteratureTitle Column/Product Application Publication Number Publication TypeReversed-Phase Separation of Intact MonoclonalAntibodies (MAb) using Agilent ZORBAX RRHD 300SB-C8


Rapid UHPLC Analysis of Reduced MonoclonalAntibodies using an Agilent ZORBAX Rapid ResolutionHigh Definition (RRHD) 300SB-C8 Column


Increased UV-Sensitivity in Combination with Novel WCX Column Separation for Better Detectability ofCharge State Variants of Biotherapeutic Proteins

Bio MAb MAbs and otherproteins

N/A Technical Poster

Agilent HPLC Column Selection Guide HPLC columns Many 5990-4435EN Selection GuideThe LC Handbook: Guide to LC Columns and Method Development

LC columns Method development 5990-7595EN Primer

Agilent PLRP-S 100Å HPLC Columns and Media PLRP-S Oligonucleotides 5990-8187EN FlyerHPLC Purification of 26-bp Serial Analysis of GeneExpression Ditags

PLRP-S Oligonucleotides 5990-7739EN Application Note

Improved Column Lifetime with Thermally Stable PolymerColumns for Oligonucleotide Ion-Pair RP HPLC


Ion-Pair Reversed-Phase Purification of De-ProtectedOligonucleotides – Choice of Pore Size


Use Temperature to Enhance Oligonucleotide MassTransfer and Improve Resolution in Ion-Pair RP HPLC


High Resolution Separations of Oligonucleotides usingPL-SAX Strong Anion-Exchange HPLC Columns

PL-SAX Oligonucleotides 5990-8297EN Application Note

Fast Impurity Profiling of Synthetic Oligonucleotides with the Agilent 1290 Infinity LC System and Agilent 6530 Accurate-Mass QTOF LC/MS

ZORBAX Eclipse Plus C18RRHD

Oligonucleotides 5990-5825EN Application Note

Agilent PLRP-S Media and Load & Lock Columns – The Future of Prep/Process Chromatography

Prep/Process Oligonucleotides,Peptides, Proteins

5990-8201EN Flyer

Agilent PLRP-S 50 µm HPLC Media PLRP-S Oligonucleotides,Peptides, Smallproteins

5990-8188EN Flyer

(Continued)

480


(Continued)

BioHPLC Columns LiteratureTitle Column/Product Application Publication Number Publication TypeAnalysis of Peptides on a PLRP-S 100Å 10 µm with ELSDetection and Acetonitrile-Free Eluents

PLRP-S Peptides 5990-7760EN Application Note

Investigation into the Alternatives to Acetonitrile for theAnalysis of Peptides

PLRP-S Peptides 5990-7740EN Application Note

Investigation into the Alternatives to Acetonitrile for theAnalysis of Peptides on a SepTech ST150 10-C18

SepTech Peptides 5990-7951EN Application Note

Investigation into the Alternatives to Acetonitrile for theAnalysis of Peptides on a VariTide RPC

VariTide RPC Peptides 5990-8145EN Application Note

Fast Monitoring of Bacteriophage Production During Fermentation Using the Agilent Bio-MonolithHPLC Column

Bio-Monolith Phage production,process monitoring

5990-3247EN Application Note

Physicochemical Characterization of a TherapeuticProtein by Peptide Mapping, SEC and IEX using theAgilent 1260 Infinity Bio-inert Quaternary LC System

Bio MAb, Bio SEC, ZORBAX Eclipse Plus,Poroshell 120

Protein analysis 5990-6192EN Application Note

Optimization of the Agilent 1100 HPLC System forSuperior Results with ZORBAX Poroshell Columns

Poroshell 300 Protein analysis 5988-9998EN Application Note

Using Poroshell 300SB-C18 for High-Sensitivity, High-Throughput Protein Analysis on the Agilent LC/MSD

Poroshell 300-C18 Protein analysis 5988-7031EN Application Note

Analysis of Albumin Proteins using ProSEC 300S Columns ProSEC 300S Protein analysis 5990-7852EN Application NoteAnalysis of Complex Bacterial Cell Division Proteins bySize Exclusion Chromatography (SEC)

ProSEC 300S Protein analysis 5990-8143EN Application Note

Analysis of Globulins using ProSEC 300S Columns ProSEC 300S Protein analysis 5990-7851EN Application NoteAnalysis of Hsp47, a Collagen Chaperone, by SizeExclusion Chromatography (SEC)


Analysis of Various Globular Proteins using ProSEC 300S Columns


Effect of pH on Protein Size Exclusion Chromatography ProSEC 300S Protein analysis 5990-8138EN Application NoteGlobular Proteins and the Calibration of ProSEC 300S Columns




Reduce Tubing Volume to Optimize Column Performance Small diameter columns Optimizing instrumentperformance


Using the High-pH Stability of ZORBAX Poroshell300Extend-C18 to Increase Signal-to-Noise in LC/MS

ZORBAX 300 Extend-C18 Optimizing instrumentperformance


Increase Sensitivity with Microbore Polymeric HPLCColumns from Agilent

PLRP-S (Microbore) Peptide hormone,small proteins, smallmolecules

5990-8666EN Technical Overview

Decreasing Analysis Time Using Poroshell 300SB-C18 inAnalysis of a Protein Digest

Poroshell 300 Peptide mapping 5988-6081EN Application Note

Rapid Peptide Mapping Method with High Resolutionusing a sub 2-µm Column

ZORBAX 300SB-C18 Peptide mapping 5990-4712EN Application Note

Increased Peak Capacity for Peptide Analysis with theAgilent 1290 Infinity LC System

ZORBAX Eclipse Plus Peptide mapping 5990-6313EN Application Note

Trypsin-Digested Monoclonal Antibody and BSA usingAgilent ZORBAX RRHD 300SB-C18

ZORBAX RRHD 300SB-C18 Peptide mapping 5990-8244EN Application Note

Preparative Scale Purification of Bradykinin byConcentration Overload

PLRP-S Peptide purification 5990-7736EN Application Note

Preparative Scale Purification of Bradykinin by Volume Overload


Preparative Scale Purification of Depherelin byConcentration Overload


Preparative Scale Purification of Leuprolide byConcentration Overload


Superior Resolution of Peptides on SepTech ST150 10-C18 using Acetonitrile-Free Gradient Elution

SepTech Peptide purification 5990-7761EN Application Note

Agilent PLRP-S Media for HPLC Analysis of Peptides PLRP-S Peptides 5990-8667EN Technical Overview



(Continued)

482


Light Scattering Analysis of BSA with ProSEC 300S Columns


Static Light Scattering Analysis of Globular Proteins with Agilent ProSEC 300S Columns


LC Handbook and Compliance Guide to RecombinantProtein Characterization

N/A Protein analysis 5990-8561EN Primer

Agilent ZORBAX 300SB-C18 1.8µm Rapid ResolutionHigh Definition Columns for Proteins

ZORBAX 300SB-C18 Protein analysis 5990-7989EN Technical Overview

Analysis of Oxidized Insulin Chains using Reversed-Phase Agilent ZORBAX RRHD 300SB-C18

ZORBAX RRHD 300SB-C18 Protein analysis 5990-7988EN Application Note

Fast Separation of Recombinant Human Erythropoietinusing Reversed-Phase Agilent ZORBAX RRHD 300SB-C18, 1.8 µm

ZORBAX RRHD 300SB-C18 Protein analysis 5990-9248EN Application Note

ACN-free HPLC Analysis and Prep Purification of ACP Fragment

PLRP-S Protein purification 5990-7762EN Application Note

Isocratic Purification of Synthetic Acyl Carrier Protein Fragment 65-74

PLRP-S Protein purification 5990-7737EN Application Note

Agilent PL-SAX Anion-Exchange Media forAmyloglucosidase Purification and Analysis

PL-SAX Protein purification 5990-8664EN Technical Overview

Progressive Denaturation of Globular Proteins in Urea ProSEC 300S Protein purification 5990-8141EN Application NoteOptimizing Protein Separations with Agilent Weak Cation-Exchange Columns

Bio IEX Protein separation 5990-9628EN Application Note

Faster Separations Using Agilent Weak Cation-Exchange Columns

Bio IEX Protein separation 5990-9931EN Application Note

Optimum Pore Size for Characterizing Biomolecules with Agilent Bio SEC Columns

Bio SEC Protein separation 5990-9894EN Application Note

Separation of High MW Fibrous Proteins PLRP-S Protein separation 5990-8137EN Application Note



(Continued)



Fast Protein Separations Using Agilent Poroshell 300 Poroshell 300 Protein separation 5989-9899EN Application NoteFast Separation of Large and Heterogeneous Proteinsusing ZORBAX Poroshell C18, C8, and C3 Phases

Poroshell 300 Protein separation 5989-0015EN Application Note

Protein Identification and Impurity Profiling using Wide-Pore Reversed-Phase HPLC/UHPLC

Poroshell 300 Protein separation 5991-0625EN Brochure

Use of Temperature to Increase Resolution in theUltrafast HPLC Separation of Proteins with ZORBAX Poroshell 300SB-C8 HPLC Columns

Poroshell 300-C8 Protein separation 5989-0589EN Application Note

The Effect of NaCl Concentration on Protein SizeExclusion Chromatography

ProSEC 300S Protein separation 5990-8139EN Application Note

The Effect of Temperature on Protein Size ExclusionChromatography

ProSEC 300S Protein separation 5990-8140EN Application Note

Infinitely Better for Bio-Molecule Analysis Agilent 1260 Infinity Bio-inert Quaternary LC System

Proteins 5990-6220EN Brochure

Defining the Optimum Parameters for Efficient SizeSeparations of Proteins

Bio SEC Proteins 5990-8832EN Technical Poster

Defining the Optimum Parameters for Efficient SizeSeparations of Proteins

Bio SEC Proteins 5990-8895EN Application Note

Compliance for Biopharmaceutical Laboratories Many Proteins 5990-7001EN PrimerGradient Purification of Synthetic Acyl Carrier ProteinFragment 65-74

PLRP-S Proteins 5990-7738EN Application Note

Fast Agilent HPLC for Large Biomolecules PLRP-S, PL-SAX, PL-SCX Proteins 5990-8663EN Technical OverviewAgilent Anion-Exchange Media for Proteins – Loading vs Resolution – Effect of Flow Rate and Example Protein Separations

PL-SAX Proteins 5990-8777EN Technical Overview

Purity Assessment Following Affinity Separation PL-SAX Proteins 5990-8436EN Technical OverviewAgilent PL-SCX Cation-Exchange Media for Large Biomolecules

PL-SCX Proteins 5990-8665EN Technical Overview



(Continued)

484


Poroshell 300SB-C18 for Fast, High Protein Separation Poroshell 300 Proteins 5988-2100ENUS BrochureProgressive Denaturation of Globular Proteins in Urea ProSEC 300S Proteins 5990-8141EN Application NoteProSEC 300S Columns Protein Characterization Columns ProSEC 300S Proteins 5990-7468EN FlyerStatic Light Scattering Analysis of Globular Proteins with Agilent ProSEC 300S Columns

ProSEC 300S Proteins 5990-7939EN Application Note

Confidently Separate and Characterize Biomolecules with Agilent BioHPLC Columns

Bio SEC, Bio IEX, Bio MAb Proteins 5990-5195EN Brochure

Increase your Productivity with Agilent ZORBAX RRHD 300Å 1.8 µm Columns

ZORBAX RRHD 300SB-C18,C8

Proteins, Peptides 5990-8124EN Flyer

High Purity, High Recovery, High Throughput – Agilent Technologies Offers Two New Lines of Preparative HPLC Columns

Agilent Prep HT Purification/Prep 5989-2350EN Brochure

Biomolecule Purification – Purification Columns and Media for Peptides, Oligonucleotides, and Proteins

PLRP-S, PL-SAX, PL-SCX Purification/Prep 5990-8335EN Brochure

The Influence of Silica Pore Size on Efficiency, Resolutionand Loading in Reversed-Phase HPLC

SepTech Purification/Prep 5990-8298EN Application Note

Analysis of Protein Primary Structure when using Wide-Pore sub-2-µm Particles and UHPLC

ZORBAX RRHD 300SB-C18 Purification/Prep 5990-8830EN Technical Poster

Polyethylene Glycol/Oxide Standards and the Calibration of Agilent ProSEC 300S Columns

ProSEC 300S SEC 5990-8147EN Application Note



TIPS & TOOLS

For the latest application notes and new product information, go towww.agilent.com/chem/library


ZORBAX 300 CitationsPortelius, E. et al. (2007) Characterization of Amyloid b Peptides inCerebrospinal Fluid by an Automated Immunoprecipitation ProcedureFollowed by Mass Spectrometry. Journal of Proteome Research, 6(11): 4433-4439Montes-Bayon, M. et al. (2006) Direct comparison of capillaryelectrophoresis and capillary liquid chromatography hyphenated tocollision-cell inductively coupled plasma mass spectrometry for theinvestigation of Cd-, Cu- and Zn-containing metalloproteins. Journal ofChromatography A, 1114(1): 138-144Zahariev, S. et al. (2006) Synthesis of ‘difficult’ peptides free ofaspartimide and related products, using peptoid methodology.Tetrahedron Letters, 47(25): 4121-4124Kohler, M. et al. (2009) Identification of Human Pituitary GrowthHormone Variants by Mass Spectrometry. Journal of ProteomeResearch, 8(2): 1071-1076Berg, M. et al. (2006) Reproducibility of LC-MS-based proteinidentification. Journal of Experimental Botany, 57(7): 1509-1514Esteban-Fernández, D. et al. (2008) Atomic (HPLC-ICP-MS) andmolecular mass spectrometry (ESI-Q-TOF) to study cis-platininteractions with serum proteins. Journal of Analytical AtomicSpectrometry, 23: 378-384Everberg, H. et al. (2006) Aqueous Two-Phase Partitioning forProteomic Monitoring of Cell Surface Biomarkers in Human PeripheralBlood Mononuclear Cells. Journal of Proteome Research, 5(5): 1168-1175Portelius, E. et al. (2010) Identification of novel N-terminal fragmentsof amyloid precursor protein in cerebrospinal fluid. ExperimentalNeurology, 223(2): 351-358Ahrends, R. et al. (2009) Metal-Coded Affinity Tag Labeling: ADemonstration of Analytical Robustness and Suitability for BiologicalApplications. Analytical Chemistry, 81(6): 2176-2184Bíliková, K. et al. (2009) Towards functional proteomics of minoritycomponent of honeybee royal jelly: The effect of post-translationalmodifications on the antimicrobial activity of apalbumin2. Proteomics,9(8): 2131-2138Schwab, K. et al. (2011) Adaptation of proteomic techniques for theidentification and characterization of protein species from murine heart.Amino Acids, 41(2): 401-414Perreault, A. et al. (2009) A Methyltransferase-independent Functionfor Rmt3 in Ribosomal Subunit Homeostasis. The Journal of BiologicalChemistry, 284: 15026-15037

Magherini, F. et al. (2009) Different carbon sources affect lifespan andprotein redox state during Saccharomyces cerevisiae chronologicalageing. Cellular and Molecular Life Sciences, 66(5): 933-947Cao H. & Xu S-Y. (2008) Purification and characterization of type IIcollagen from chick sternal cartilage. Food Chemistry, 108(2): 439-445Chen, X. et al. (2010) Quantitative Proteomics Analysis of Cell Cycle-regulated Golgi Disassembly and Reassembly. The Journal of BiologicalChemistry, 285: 7197-7207Trusch, M. et al. (2010) Application of displacement chromatographyfor the analysis of a lipid raft proteome. Journal of Chromatography B,878(3-4): 309-314Amoresano, A. et al. (2008) A Rapid and Selective Mass SpectrometricMethod for the Identification of Nitrated Proteins. Methods inMolecular Biology, 477(I): 15-29Kodali, VP., Das, S. & Sen, R. (2009) An exopolysaccharide from aprobiotic: Biosynthesis dynamics, composition and emulsifying activity.Food Research International, 42(5-6): 695-699Loeber, R. et al. (2008) Cross-Linking of the DNA Repair Protein O6-Alkylguanine DNA Alkyltransferase to DNA in the Presence ofAntitumor Nitrogen Mustards. Chemical Research in Toxicology, 21(4):787-795

Citations

Millette, M. et al. (2008) Purification and identification of the pediocinproduced by Pediococcus acidilactici MM33, a new human intestinalstrain. Journal of Applied Microbiology, 104(1): 269-275Chen, X. et al. (2009) Quantitative Organellar Proteomics Analysis ofRough Endoplasmic Reticulum from Normal and Acute Pancreatitis RatPancreas. Journal of Proteome Research, 9(2): 885-896Ameri, M., Daddona, P. & Maa, YF. (2009) Demonstrated Solid-StateStability of Parathyroid Hormone PTH(1–34) Coated on a NovelTransdermal Microprojection Delivery System. PharmaceuticalResearch, 26(11): 2454-2463Gianazza, E. et al. (2010) Different expression of Fibrinopeptide A andrelated fragments in serum of type 1 diabetic patients withnephropathy. Journal of Proteomics, 73(3): 593-601Yuan, W. et al. (2008) Two New Holostan-Type Triterpene Glycosidesfrom the Sea Cucumber Bohadschia marmorata JAEGER. Chemical &Pharmaceutical Bulletin, 56(8): 1207


486


Poroshell 300 CitationsMatilainen, L. et al. (2008) The effect of cyclodextrins on chemical andphysical stability of glucagon and characterization of glucagon/g-CDinclusion complexes. Journal of Pharmaceutical Sciences, 97(7): 2720-2729Astarita, G., Ahmed, F. & Piomelli, D. (2008) Identification ofbiosynthetic precursors for the endocannabinoid anandamide in the ratbrain. The Journal of Lipid Research, 49: 48-57Matilainen, L. et al. (2008) The stability and dissolution properties ofsolid glucagon/g-cyclodextrin powder. European Journal ofPharmaceutical Sciences, 36(4-5): 412-420Wang, Y. et al. (2009) Comparison of Methods for Extracting KafirinProteins from Sorghum Distillers Dried Grains with Solubles. Journal ofAgricultural & Food Chemistry, 57(18): 8366-8372Guerrera, IC. et al. (2009) A Novel Lipidomic Strategy Reveals PlasmaPhospholipid Signatures Associated with Respiratory Disease Severityin Cystic Fibrosis Patients. PLoS ONE, 4(11): e7735Yung, KM. et al. (2011) An amyloid b42-dependent deficit inanandamide mobilization is associated with cognitive dysfunction inAlzheimer's disease. Neurobiology of AgingReid, CQ. et al. (2010) Rapid whole monoclonal antibody analysis bymass spectrometry: An Ultra scale-down study of the effect ofharvesting by centrifugation on the post-translational modificationprofile. Biotechnology and Bioengineering, 107(1): 85-95Heinig, K. & Wirz, T. (2009) Determination of Taspoglutide in Humanand Animal Plasma Using Liquid Chromatography − Tandem MassSpectrometry with Orthogonal Column-Switching. Analytical Chemistry,81(10): 3705-3713Rossi, EA. et al. (2010) A Bispecific Antibody-IFNa2b ImmunocytokineTargeting CD20 and HLA-DR Is Highly Toxic to Human Lymphoma andMultiple Myeloma Cells. Cancer Research, 70: 7600Murphy, MP. et al. (2010) Changes in Cognition and Amyloid-bProcessing with Long Term Cholesterol Reduction using Atorvastatin inAged Dogs. Journal of Alzheimer's Disease, 22(1): 135-150

PLRP-S CitationsNakagawa, M., Tojo, H. & Fujii, S. (2011) A Glycan of Y-Factor fromDictyostelium discoideum Contains a Bisecting-GlcNAc, anIntersecting-GlcNAc, and a Core a-1,6-Fucose. Bioscience,Biotechnology, and Biochemistry, 75(10):1964-1970Della Donna, L. et al. (2011) Mass spectrometric measurements of theapolipoproteins of bovine (Bos taurus) HDL. Comparative Biochemistryand Physiology Part D: Genomics and ProteomicsVondenhoff, GHM. et al. (2011) Characterization of Peptide ChainLength and Constituency Requirements for YejABEF-Mediated Uptakeof Microcin C Analogues. The Journal of Bacteriology, 193(14): 3618-3623Šotkovský, P. et al. (2011) A new approach to the isolation andcharacterization of wheat flour allergens. Clinical & ExperimentalAllergy, 41(7): 1031-1043Laabs, E. et al. (2011) Optical Imaging of CCK2/Gastrin Receptor-Positive Tumors With a Minigastrin Near-Infrared Probe. InvestigativeRadiology, 46(3): 196-201Rickert, KW. et al. (2011) Structural Basis for Selective Small MoleculeKinase Inhibition of Activated c-Met. The Journal of BiologicalChemistry, 286: 11218-11225Stuknyte, M. et al. (2011) Potential immunomodulatory activity ofbovine casein hydrolysates produced after digestion with proteinasesof lactic acid bacteria. International Dairy Journal, 21(10): 63-769Nakano, E. et al. (2011) Riboflavin Depletion Impairs Cell Proliferationin Adult Human Duodenum: Identification of Potential Effectors.Digestive Diseases and Sciences, 56(4): 1007-1019Webb, K. et al. (2011) The ribosomal L1 protuberance in yeast ismethylated on a lysine residue catalyzed by a seven beta-strandmethyltransferase. The Journal of Biological Chemistry, M110. 200410Uehata, T. et al. (2011) Serum hepcidin-25 levels and anemia in non-dialysis chronic kidney disease patients: a cross-sectional study.Nephrology Dialysis Transplantation, 27(3): 1076-1083Lohman, G, Chen, L. & Evans Jr, T. (2011) Kinetic characterization of single strand break ligation in duplex DNA by T4 DNA Ligase. The Journal of Biological Chemistry, 286: 44187-44196

(Continued)



Hudak, J., Yu, H. & Bertozzi, C. (2011) Protein GlycoengineeringEnabled by the Versatile Synthesis of Aminooxy Glycans and theGenetically Encoded Aldehyde Tag. Journal of the American ChemicalSociety, 133(40): 16127-16135Schneider, N. et al. (20111) Prevalence and stability of lysozyme incheese. Food Chemistry, 128(1): 145-151 Yan, B. & Boyd, D. (2011) Breaking the Light and Heavy Chain Linkageof Human Immunoglobulin G1 (IgG1) by Radical Reactions. The Journal of Biological Chemistry, 286: 24674-24684Landau, M. et al. (2011) Towards a Pharmacophore for Amyloid. PLoSBiology, 9(6): e1001080Kerkaert, B. et al. (2011) Use of lysozyme as an indicator of proteincross-contact in fresh-cut vegetables via wash waters. Food ResearchInternational, 45(1): 39-44Schneider, N., Werkmeister, K. & Pischetsrieder, M. (2011) Analysis ofnisin A, nisin Z and their degradation products by LCMS/MS. FoodChemistry, 127(2): 847-854Quenee, L. et al. (2011) Prevention of pneumonic plague in mice, rats,guinea pigs and non-human primates with clinical grade rV10, rV10-2or F1-V vaccines. Vaccine, 29(38): 6572-6583

PLRP-S Citations PL-SAX CitationsPratto, F. et al. (2008) Streptococcus pyogenes pSM19035 requiresdynamic assembly of ATP-bound ParA and ParB on parS DNA duringplasmid segregation. Nucleic Acids Research, 3 (11): 3676-3689Sendovski, M. et al. (2010) Crystallization and preliminary X-raycrystallographic analysis of a bacterial tyrosinase from Bacillusmegaterium. Acta Crystallographica, 66(9): 1101-1103Bunger, MK. et al. (2008) Automated Proteomics of E. coli via Top-Down Electron-Transfer Dissociation Mass Spectrometry. AnalyticalChemistry, 80(5): 1459-1467Vantourout, P. et al. (2009) Specific Requirements for Vg9Vd2 T CellStimulation by a Natural Adenylated Phosphoantigen. The Journal ofImmunology, 183(6): 3848-3857Scaboo, AM. et al. (2009) Confirmation of Molecular Markers and Agronomic Traits Associated with Seed Phytate Content in Two Soybean RIL Populations. Crop Science, 49(2): 426-432

PL-SCX CitationsZhang, W. & Czupryn, M. (2003) Analysis of isoaspartate in arecombinant monoclonal antibody and its charge isoforms. Journal ofPharmaceutical and Biomedical Analysis, 30(5): 1479-1490Collinge, J. et al. (2005) Differential Proteomics via ProbabilisticPeptide Identification Scores. Analytical Chemistry, 77(2): 596-606Schönleben, S. et al. (2007) Proteome analysis of Apis mellifera royaljelly. Analytical and Bioanalytical Chemistry, 389(4): 1087-1093Lohaus, C. et al. (2007) Multidimensional Chromatography: a PowerfulTool for the Analysis of Membrane Proteins in Mouse Brain. Journal ofProteome Research, 6(1): 105-113Zahedi, RP. et al. (2007) Phosphoproteome of Resting HumanPlatelets. Journal of Proteome Research, 7(2): 526-534Boehm, A. et al. (2007) Precise protein quantification based on peptidequantification using iTRAQ™. BMC Bioinformatics, 8: 214Heller, M. et al. (2003) Trypsin catalyzed 16O-to-18O exchange forcomparative proteomics: tandem mass spectrometry comparison usingMALDI-TOF, ESI-QTOF, and ESI-ion trap mass spectrometers. Journal ofthe American Society for Mass Spectrometry, 14(7): 704-718

488

GPC/SEC ColumnS and STandardS

TiPS & ToolS

For information on SEC columnsfor proteins, turn to pages 416-417.

GPC/SEC Columns and Standards• A full portfolio of products for analysis of synthetic and natural polymers• A wide selection of polymer standards to cover the range of applications in organic and

water based solvents• PL aquagel-OH-series, for aqueous SEC separations, and PLgel, for organic polymer applications,

are available in mixed and individual pore sizes across a range of particle sizes, to cover the fullspectrum of molecular weights (MW)

• Prep scale columns are available, along with narrow bore columns and columns designed for specific applications

Gel permeation chromatography (GPC) and size exclusion chromatography (SEC) are names applied to themost popular technique for measuring the molecular weight distribution (MWD) of natural and syntheticpolymers, a property that affects many of the physical parameters of materials such as strength, toughnessand chemical resistance. GPC and SEC are liquid chromatographic techniques that separate individualpolymer chains on the basis of their size in solution and not on their chemistry. Gel permeationchromatography (GPC) is the name used to describe the analysis of polymers in organic solvents, such astetrahydrofuran. Size exclusion chromatography (SEC) is the name used to describe the analysis of polymersin water and water-based solvents, such as buffer solutions. GPC/SEC is the only established method forobtaining a comprehensive understanding of a polymer’s molecular weight distribution.

489www.aGilEnT.Com/ChEm/lC


LC and LC/MS Columns for GPC/SECTable of Contents

GPC/SEC Columns............................................................488PLgel GPC............................................................................496PLgel MIXED.......................................................................498PLgel MIXED-LS.................................................................502PLgel MiniMIX....................................................................504PLgel Individual Pore Size ................................................505PLgel Preparative...............................................................506EnviroPrep ...........................................................................507PLgel Olexis ........................................................................508PL HFIPgel...........................................................................509PL Rapide ............................................................................510PolarGel ...............................................................................512PlusPore ..............................................................................514PolyPore ..............................................................................516

ResiPore ..............................................................................518MesoPore............................................................................520OligoPore.............................................................................521PL aquagel-OH SEC ...........................................................523PL aquagel-OH SEC Analytical ........................................525PL aquagel-OH SEC Preparative......................................528GPC Column Accessories.................................................529

Polymer Standards for GPC/SEC ....................................530EasiVial ................................................................................532EasiCal .................................................................................536Polystyrene .........................................................................537Polymethylmethacrylate ...................................................539Polyethylene Glycol/Oxide...............................................541Polysaccharides .................................................................543Polyacrylic Acid..................................................................545

490


The key to successful GPC/SEC separations is the correct choice of columns. The comprehensive range ofAgilent products for GPC/SEC has been designed to cover virtually all polymer analysis application areas,and to make selection for the correct column, solvent, and calibration standard fast and reliable.

Agilent’s PLgel GPC series of columns are for polymer applications using organic solvents. PLgel is a highlycross-linked, porous polystyrene/divinylbenzene matrix, which is recognized as a market leader in GPCcolumn technology. PLgel materials have high pore volume and high-efficiency to maximize resolution. Their unequalled solvent compatability makes for easy transfer between polar and non-polar eluents, and outstanding physical rigidity provides extended lifetimes that maximize downtime. For more information and full ordering details, see

Agilent’s PL aquagel-OH series of columns provide a chemically and physically stable matrix for reliableaqueous SEC separations. The columns are packed with macroporous copolymer beads with an extremelyhydrophilic polyhydroxyl functionality. The “neutral” surface and the capability to operate across a widerange of eluent conditions provide for high performance analyses of compounds with neutral, ionic, andhydrophobic moieties, alone or in combination. PL aquagel-OH is available for analytical and preparativeapplications. For more information and full ordering details, see

GPC/SEC Columns

pages 496-497.

page 523.

Polymer standards for GPC/SECAgilent manufactures the highest quality polymer standards with extremely narrow polydispersity and thewidest molecular weight range commercially available. These quality polymer standards are supplied withextensive characterization data utilizing a variety of independent techniques (e.g. light scattering andviscometry) and high performance GPC to verify polydispersity and assign the peak molecular weight (Mp).

EasiVial – for organic and aqueous calibration. EasiVial is the fastest and most convenient method to deliveran accurate 12-point column calibration. EasiVial eliminates tedious weight procedures for improvedcalibration accuracy and reduces solvent dispensing to limit risks associated with handling solvents.

EasiCal – for organic solvents. EasiCal packs are pre-prepared for a no-fuss process. Two different combs,each with ten detachable spatulas, support a mixture of five polymer standards. The cost-effective format isdesigned to save money.

Individual standards and kits – an extensive range of polymer standard kits of different chemistries designedto match specific column sets are available, as well as individual standards in various pack sizes. For moredetails about Agilent’s calibration standards for GPC/SEC, see page 530.


• Polymer molecules dissolve in solution to form spherical coils with size dependent on molecular weight• The polymer coils are introduced to eluent flowing through the column• Columns are packed with insoluble porous beads with well-defined pore structure• The size of pores is similar to that of the polymer coils• The polymer coils diffuse in and out of the pores• Result is elution based on size – large coils first, smaller coils last• Size separation converted to molecular weight separation by use of a calibration curve constructed

by the use of polymer standards

Smaller coils can access many pores

Larger coils can access few pores

Very large coils access very few pores

Mechanisms of GPC and SEC

how GPC/SEC works:


Key

492


Choosing an eluent for GPC/SEC

Question answer recommendation Comments1. What is the sample soluble in? Water or water buffer

with up to 50% methanolAgilent PL aquagel-OH Best choice for water-based applications

but cannot accommodate organics apart frommethanol up to 50%

Many polymers are only soluble in a small number of solvents. This is the key question when developing methods for analyzing polymers.The solvents mentioned here are all commoneluents employed in GPC/SEC.

Typical organic solventsuch as THF, chloroform, toluene

Agilent PLgel orAgilent PlusPore

PLgel are the workhorse columns, PlusPore columnsare an alternative

Organic/water mixtures orpolar organics such as,DMF, NMP

Agilent PolarGel PolarGel is a smaller column range than PLgel or PL aquagel-OH columns but is suited to mixtures of organics and water

The following questions will help you find the recommended columns and standards for any given application, as well as system parameters such asinjection volumes.

TiPS & ToolS

More information on GPC/SECinstrumentation and systems is a clickaway. We have a variety of applicationnotes, data sheets and brochuresavailable from Agilent for free.

To learn more, visitwww.agilent.com/chem/gpc

recommendations for setting up a GPC/SEC system



Choosing a column for GPC/SECColumns shown in bold are the best initial choice

Question answer recommendation Comments2. What is the expected

molecular weight?High (up to several millions)

Aqueous solventsPl aquagel-oh miXEd-h 8 µmor combination ofPL aquagel-OH 40 and 60 15 µm

The 15 µm column combination is best only where sample viscosity is very high, otherwise 8 µm columns give greater resolution

It may seem strange to ask this question, but inGPC/SEC the resolution ofa column is related to theresolving range. Knowingsomething of the expectedmolecular weight of asample helps to choose thebest column that will giveoptimum results.

Organic solventsPlgel 10 µm miXEd-B orPLgel 20 µm MIXED-A

The PLgel MIXED-A column resolves higher than the PLgelMIXED-B but at lower efficiency due to larger particle size

Mixed solventsPolarGel

No PolarGel column available for this molecular weight range.Contact your local GPC/SEC expert for advice

Intermediate (up tohundreds ofthousands)

Aqueous solventsPl aquagel-oh miXEd-m 8 µm

A wide-ranging column that covers most water-soluble polymers

Organic solventsPlgel 5 µm miXEd-C orPLgel 5 µm MIXED-D, PolyPoreor ResiPore

The PLgel columns are the most widely applicable for the majority of applications; PolyPore and ResiPore columnsare alternatives

Mixed solventsPolarGel-m

Covers most applications

Low (up to tens ofthousands)

Aqueous solventsCombination of Pl aquagel-oh 40and Pl aquagel-oh 30 8 µm

These two columns in a combined set cover the low end of the molecular weight range

Organic solventsPlgel 3 µm miXEd-Eor MesoPore

The PLgel column provides high resolution and is designed for low molecular weight applications; the MesoPore columnis an alternative

Mixed solventsPolarGel-l

For low molecular weight applications

Very low (a fewthousand)

Aqueous solventsPl aquagel-oh 20 5 µm

This high-performance column gives high resolution at lowmolecular weight

Organic solventsoligoPore or PLgel 3 µm 100Å

The OligoPore column is less prone to dispersion than thePLgel column, but both work well

Mixed solventsPlgel

No PolarGel column covers this range so use PLgel columns as alternatives

Unknown Aqueous solventsPl aquagel-oh miXEd-m 8 µm

Covers the molecular weight ranges of most polymer samples

Organic solventsPlgel 5 µm miXEd-C or PolyPore

This PLgel column is the most widely applicable for themajority of applications

Mixed solventsPolarGel-m

Covers the majority of applications

494


Setting up the GPC/SEC system

Question answer recommendation Comments3. How many columns to use? Depends on the particle

size of the columnsParticle size 20 µm use 4 columns Increased number of columns required

for large particle sizes to make up forlow efficiencies

The greater the particle size of themedia in the column (which isdependent on the expectedmolecular weight of the samples), thelower the resolution and the morecolumns are required to maintain thequality of the results. For highermolecular weight samples, largerparticles are necessary to reduce thedanger of shear degradation ofsamples during analysis.

Particle size 13 µm use 3 columnsParticle size 10 µm use 3 columnsParticle size 8 µm use 2 columnsParticle size 5 µm use 2 columnsParticle size 3 µm use 2 columns

Question answer recommendation Comments4. What size injection volume? Depends on the particle

size of the columnsParticle size 20 µm use 200 µL injection Smaller particle sizes require smaller

loops to minimize band broadeningThe injection volume required isdependent on the particle size of thecolumn – smaller particles needlower injection volumes to minimizedead volume. Larger injectionvolumes allow the introduction ofhigh molecular weight samples atlower concentrations, reducingviscosity and ensuring a qualitychromatogram is obtained.

Particle size 13 µm use 200 µL injectionParticle size 10 µm use 200 µL injectionParticle size 5 µm use 100 to 200 µL injectionParticle size 3 µm use 20 µL injection

what standards should i use?Standards shown in bold are the best initial choice

Question answer recommendation Comments5. What is the eluent? Water or water buffer with up to 50%

methanolPolyethylene glycol (PEG)/oxide(PEo) or polysaccharides (SAC)

These standards perform in all water-based systems, PEG/PEO inconvenient Agilent EasiVial format

Standards are polymers, so the choice of standard mainly reflectssolubility in the chosen eluents.

Typical organic solvent such as THF,chloroform, toluene

Polystyrene (PS) orpolymethylmethacrylate (PMMA)

Polystyrene is the most commonlyused standard in convenient EasiVial format

Organic/water mixtures or polarorganics such as DMF, NMP

Polyethylene glycol/oxide orpolymethylmethacrylate

Polar standards perform well

(Continued)



Typical polymer molecular weightsIf you are unsure of the molecular weight of your sample, the table below shows some approximate molecular weight ranges for common polymers, which willhelp you select the right column for your application.

Polymer Type Typical molecular weight of polymerTypical polydispersity1

of polymer

Polymers from free radical synthesisHigh (up to several million)

~ 2Intermediate (up to hundreds of thousands)

Polymers from ionic synthesisIntermediate (up to hundreds of thousands)

~ 1.01Low (up to tens of thousands)

Polymers from addition synthesisIntermediate (up to hundreds of thousands)

~ 2Low (up to tens of thousands)

Polymers from controlled radical polymerizationLow (up to tens of thousands)

~ 1.1 to 1.5Very low (a few thousand)

PolyolefinsIntermediate (up to hundreds of thousands)

~ 2 to 200High (up to several million)

AcrylatesIntermediate (up to hundreds of thousands)

~ 2High (up to several million)

Small molecule additives Very low (a few thousand) 1

Pre-polymersLow (up to tens of thousands)

~ 2 to 10Very low (a few thousand)

ResinsLow (up to tens of thousands)

~ 2 to 10Very low (a few thousand)

Natural biopolymers such as polysaccharidesIntermediate (up to hundreds of thousands)


RubbersIntermediate (up to hundreds of thousands)


Biodegradable polymersIntermediate (up to hundreds of thousands)

~ 1.1 to 2Low (up to tens of thousands)

1 Polydispersity is a measure of the distribution of molecular mass of a polymer. Polydispersity index (PDI) = Mw/Mn.

Question answer recommendation Comments6. What format of standards are recommended?

For the quickest and simplest approachwhere accurate concentrations are not required

Easiest option – EasiVial or EasiCal Simple to use, EasiVial preferredbefore EasiCal because of the widerchoice of polymer types

Different formats of standards are available depending on customer preference.

If accurate concentrations are required Accurate concentrations required –EasiVial or individual standards

Both formats allow accurate sampleconcentrations, EasiVials are simplerto use

what standards should i use?

496


Organic GPCPlgel GPC Columns• Robust performance under the most exacting conditions• Temperature stability up to 220 °C• Solvent compatibility allows easy and rapid transfer between solvents of varying polarity

PLgel materials have high pore volume and high efficiency to maximize resolution. Their unequalled solventcompatibility makes for easy transfer between polar and non-polar eluents, and outstanding physical rigidityprovides extended lifetimes that minimize downtime.

The key to successful GPC separations is the correct choice of columns. The comprehensive range of PLgelproducts has been designed to cover virtually all organic solvent-based polymer analysis application areas,and to make selection of the correct column, solvent, and calibration standard fast and reliable.

PLgel is a highly cross-linked, porous polystyrene/divinylbenzene matrix, which is recognized as a market leader in GPC column technology. PLgel is manufactured to ISO 9001:2000 and benefits from comprehensive QC/QA for total reproducibility, batch-to-batch and column-to-column.



Plgel is compatible with all of these solvents

Solvent Polarity Solvent6.0 Perfluoroalkane7.3 Hexane8.2 Cyclohexane8.9 Toluene9.1 Ethyl acetate9.1 Tetrahydrofuran (THF)9.3 Chloroform9.3 Methyl ethyl ketone (MEK)9.7 Dichloromethane9.8 Dichloroethene9.9 Acetone10.0 o-Dichlorobenzene (o-DCB)10.0 Trichlorobenzene (TCB)10.2 m-Cresol10.2 o-Chlorophenol (o-CP)10.7 Pyridine10.8 Dimethyl acetamide (DMAc)11.3 n-Methyl pyrolidone (NMP)12.0 Dimethyl sulfoxide (DMSO)12.1 Dimethyl formamide (DMF)

*We also provide a custom packing service in which columns can be shipped in specific solvents to provide extraconvenience to our customers.

Solvent CompatibilityPLgel columns are routinely supplied in ethyl benzene* but you can easily and rapidly transfer betweensolvents of varying polarity. In organic GPC, sample to column interaction may occur occasionally and eluentmodification can be used to eliminate these effects. PLgel columns are the ideal choice for such analyses, asthey easily tolerate eluents in the pH range 1-14, as well as up to 10% water in a miscible organic solvent.

Plgel Frit Porosity

media Type Porosity (µm)PLgel 3 µm 2PLgel 5 µm 2PLgel 10 µm 5PLgel 20 µm 10

page 529For Plgel column accessories ordering information please see

498


Plgel miXEd Columns


Column

linear mwoperating range(g/mol)

GuaranteedColumn Efficiency

TypicalPressure

maximumFlow rate

maximumPressure

maximumTemperature

PLgel MIXED-A 2,000-40,000,000 > 17,000 p/m 1 mL/min (7.5 mm id):≈ 3 bar (44 psi) per 300 mm0.3 mL/min (4.6 mm id):≈ 2.4 bar (35 psi) per 250 mm(THF @ 20 °C, TCB @ 140 °C)

7.5 mm id: 1.5 mL/min4.6 mm id: 0.5 mL/min

150 bar(2175 psi)

220 °C

PLgel MIXED-B 500-10,000,000 > 35,000 p/m 1 mL/min (7.5 mm id):≈ 10 bar (145 psi) per 300 mm0.3 mL/min (4.6 mm id):≈ 8 bar (116 psi) per 250 mm(THF @ 20 °C, TCB @ 140 °C)


150 bar(2175 psi)

220 °C

PLgel MIXED-C 200-2,000,000 > 50,000 p/m 1 mL/min (7.5 mm id):≈ 30 bar (435 psi) per 300 mm0.3 mL/min (4.6 mm id):≈ 24 bar (348 psi) per 250 mm(THF @ 20 °C, TCB @ 140 °C)


150 bar(2175 psi)

150 °C

PLgel MIXED-D 200-400,000 > 50,000 p/m 1 mL/min (7.5 mm id):≈ 30 bar (435 psi) per 300 mm0.3 mL/min (4.6 mm id):≈ 24 bar (348 psi) per 250 mm(THF @ 20 °C, TCB @ 140 °C)


150 bar(2175 psi)

150 °C

PLgel MIXED-E up to 30,000 7.5 x 300 mm: > 80,000 p/m4.6 x 250 mm: > 70,000 p/m

1 mL/min (7.5 mm id):≈ 50 bar (725 psi) per 300 mm0.3 mL/min (4.6 mm id):≈ 42 bar (609 psi) per 250 mm(THF @ 20 °C)


180 bar(2611 psi)

110 °C

The PLgel MIXED range greatly simplifies column selection for easy decision making. By using these mixed columns, you can eliminate mismatched columnsets and spurious peaks for more reliable results. Every column contains a mixture of individual pore size materials, accurately blended to cover a specifiedbroad range of molecular weight with a linear calibration to eliminate column mismatch. Simply add extra columns for even greater resolution.



Reference: Meehan, E. (1998) Size exclusion chromatography columns from Polymer Laboratories. In:Chi-San Wu (Ed.) Column Handbook for Size Exclusion Chromatography. Academic Press, New York, USA.

4

1 K

10 M

10

VLC0014

uhmw polymer distributions

Plgel miXEd Column Selection Guide

high mw polymers, demanding eluents

mid range mw polymers, high resolution

resins, condensation polymers

low mw resins, prepolymers

PLgel MIXED-A, 20 µm

PLgel MIXED-B, 10 µm

PLgel MIXED-C, 5 µm

PLgel MIXED-D, 5 µm

PLgel MIXED-E, 3 µm

102MW 107

Plgel miXEd Gel Calibration CurvesMIXED gel calibration curves are designed to be linear over a specified molecular weight range, ensuring that the same degree of resolution is achievedacross the full operating range of the column. The particle size of the packing and porosity of a particular MIXED gel column are carefully matched to theMW range and application, thus optimizing performance and eliminating the effects of shear degradation. Resolution in GPC is controlled by the slope of the calibration curve and the particle size of the packing material. Agilent has scientifically determined the minimum number of MIXED gel columns requiredto perform accurate MWD determinations based on specific resolution (Rsp). Thus you can have complete confidence in the accuracy and precision of thecalculated data.

Key

Elution Volume (mL)

Polys

tyren

e Mole

cular

Weig

ht

PLgel MIXED-A, 20 µm

PLgel MIXED-B, 10 µm

PLgel MIXED-C, 5 µm

PLgel MIXED-D, 5 µm

PLgel MIXED-E, 3 µm

500


Plgel miXEd Columnsdescription Size (mm) Part no.PLgel 20 µm MIXED-A 7.5 x 300 PL1110-6200PLgel 10 µm MIXED-B 7.5 x 300 PL1110-6100PLgel 5 µm MIXED-C 7.5 x 300 PL1110-6500PLgel 5 µm MIXED-D 7.5 x 300 PL1110-6504PLgel 3 µm MIXED-E 7.5 x 300 PL1110-6300

Plgel miXEd GuardsSize (mm) Particle Size (µm) Part no.7.5 x 50 20 PL1110-12207.5 x 50 10 PL1110-11207.5 x 50 5 PL1110-15207.5 x 50 3 PL1110-1320

StarchesColumn: 4 x Plgel 20 µm miXEd-a

Pl1110-62007.5 x 300 mm

Mobile Phase: DMSO + 5 mM NaNO3


Temperature: 80 °C

Detector: RI

Polyphenylene SulfidesColumn: 3 x Plgel 10 µm miXEd-B

Pl1110-61007.5 x 300 mm

Mobile Phase: o-Chloronaphthalene


Temperature: 210 °C

Detector: RI



Plasticized PVCColumn: 3 x Plgel 5 µm miXEd-C

Pl1110-65007.5 x 300 mm

Mobile Phase: THF


Detector: RI

Epoxy resinColumn: 3 x Plgel 5 µm miXEd-d

Pl1110-65047.5 x 300 mm

Mobile Phase: THF


Detector: RI

PolyolColumn: Plgel 3 µm miXEd-E

Pl1110-63007.5 x 300 mm

Mobile Phase: THF



502


• Obtain an instant improvement in data quality• No need for conditioning, saving time and solvent costs• Maximize the potential of light scattering detectors

The PLgel MIXED-LS series is a PS/DVB packing using an innovative proprietary suspension polymerizationtechnique to virtually eliminate nano-particle leakage. A startling improvement is achieved immediately inthe quality of light scattering data obtained with PLgel MIXED-LS columns in place of conventional GPCcolumns. The light scattering chromatograms shown here were obtained after flushing the columns for one hour in THF at 1 mL/min. A polystyrene standard (Mp 210,000) was injected at 1 mg/mL in order to illustrate the dramatic improvement in signal-to-noise with the PLgel MIXED-LS column.

The performance of PLgel MIXED-LS columns has been matched to PLgel 20 µm MIXED-A and PLgel 10 µmMIXED-B columns in terms of calibration, column efficiency, wide solvent compatibility, and operatingtemperature. MIXED-LS are also ideal for online viscosity detection, minimizing the risk of capillary blockage,and can be used with regular PLgel guard columns that are packed with rigid low pore size gels with noparticle bleed.

Plgel miXEd-lS Columns

description Size (mm)

linear mwoperating range

(g/mol) (PS)

GuaranteedEfficiency

(p/m) Part no.PLgel 10 µm MIXED-B LS 7.5 x 300 500-10,000,000 >35,000 PL1110-6100LSPLgel 10 µm guard 7.5 x 50 PL1110-1120PLgel 20 µm MIXED-A LS 7.5 x 300 2,000-40,000,000 >17,000 PL1110-6200LSPLgel 20 µm guard 7.5 x 50 PL1110-1220

Plgel miXEd-lS Columns


Conventional GPC columnColumn: Conventional GPC columnMobile Phase: THF


Detector: LS

Plgel lS columnColumn: Plgel 10 µm miXEd-B lS

Pl1110-6100lS7.5 x 300 mm, 10 µm

Mobile Phase: THF


Detector: LS

VLC001560 min 70

60 min 70


Light scattering detection with a PLgel LS column – minimal particulate bleed gives greatlyimproved baseline.

Light scattering detection with a conventional GPC column – noise due to particulate bleed.

504


• Use about 70% less solvent and save money• Store less solvent and increase operator safety• High performance comparable to Agilent's conventional id columns

For reduced solvent cost and consumption, use industry standard PLgel MiniMIX mixed gel columns in 250 x 4.6 mm narrow bore dimensions. These narrow bore columns offer high performance, excellentsolvent compatibility and mechanical stability. PLgel MiniMIX columns can be used with conventional GPC equipment.

To maintain the same linear velocity through the column, the volumetric flow rate must be reduced to 0.3 mL/min in line with the column cross sectional area, resulting in significantly lower solvent consumption.Sample loading should also be scaled down in line with reduced column volume, and system dead volumeshould be minimized to avoid excessive band broadening.

Plgel minimiX Columns

descriptionSize(mm)


(g/mol) (PS)


(p/m) Part no.PLgel 20 µm MiniMIX-A 4.6 x 250 2,000-40,000,000 > 17,000 PL1510-5200PLgel 20 µm MiniMIX-A guard 4.6 x 50 PL1510-1200PLgel 10 µm MiniMIX-B 4.6 x 250 500-10,000,000 > 35,000 PL1510-5100Plgel 10 µm MiniMIX-B guard 4.6 x 50 PL1510-1100PLgel 5 µm MiniMIX-C 4.6 x 250 200-2,000,000 > 50,000 PL1510-5500PLgel 5 µm MiniMIX-C guard 4.6 x 50 PL1510-1500PLgel 5 µm MiniMIX-D 4.6 x 250 200-400,000 > 50,000 PL1510-5504PLgel 5 µm MiniMIX-D guard 4.6 x 50 PL1510-1504PLgel 3 µm MiniMIX-E 4.6 x 250 up to 30,000 > 70,000 PL1510-5300PLgel 3 µm MiniMIX-E guard 4.6 x 50 PL1510-1300

Plgel minimiX Columns


Plgel individual Pore Size Columns• Very high efficiency improves productivity• Choose the optimum column for a perfect match of performance and application• Fast analysis with fewer columns saves time and money

Individual pore size GPC columns offer high resolution over a specific molecular weight range. The linearportion of the calibration curve, where the slope is at its shallowest, defines the MW region over whichoptimum resolution will be achieved.

Plgel individual Pore Size Columns

Size (mm)

ParticleSize(µm)

Pore Size(Å)


(g/mol) (PS)


(p/m) Part no.7.5 x 300 3 100 up to 4,000 > 100,000 PL1110-63207.5 x 300 5 50 up to 2,000 > 60,000 PL1110-65157.5 x 300 5 100 up to 4,000 > 60,000 PL1110-65207.5 x 300 5 500 500-30,000 > 60,000 PL1110-65257.5 x 300 5 103 500-60,000 > 50,000 PL1110-65307.5 x 300 5 104 10,000-600,000 > 50,000 PL1110-65407.5 x 300 5 105 60,000-2,000,000 > 50,000 PL1110-65507.5 x 300 10 50 up to 2,000 > 35,000 PL1110-61157.5 x 300 10 100 up to 4,000 > 35,000 PL1110-61207.5 x 300 10 500 500-30,000 > 35,000 PL1110-61257.5 x 300 10 103 500-60,000 > 35,000 PL1110-61307.5 x 300 10 104 10,000-600,000 > 35,000 PL1110-61407.5 x 300 10 105 60,000-2,000,000 > 35,000 PL1110-61507.5 x 300 10 106 600,000-10,000,000 > 35,000 PL1110-6160PLgel Guard Column information can be found on page 500

Calibration curvesCalibrant: Polystyrene

Mobile Phase: THF


4

1 K

10 M

106Å

105Å

104Å

103Å

500Å

100Å

50Å

10VLC0016

Polys

tyren

e Mole

cular

Weig

ht

Elution Volume (mL)


506


• Excellent column efficiency provides optimum resolution• High loading can isolate mg amounts for further study• Over 10 times scale up permits efficient quantification

Preparative GPC is generally employed to fractionate polymers, isolate components in a polymer formulation or simplify mixtures of relatively small molecules in complex matrices. Mixtures of materials are easily separated on the basis of size, preferably in a low boiling organic solvent. They are then collectedas a series of discrete fractions and isolated by simple evaporation of the solvent.

PLgel preparative columns are packed with the same rigid, high performance media as the analyticalcolumns. The 10 µm particle provides high column efficiency (> 25,000 p/m) for optimum resolution andloading characteristics. PLgel 25 mm id preparative columns offer over 10 times scale-up compared to the7.5 mm analytical columns. The increased id and column volume permit even higher loading. With lowmolecular weight materials, sample concentration can also be significantly increased, enabling productionof milligram quantities of very pure material. The actual loading is ultimately controlled by the sample and itsmolecular weight.

Plgel Preparative Columns

Size (mm) Particle Size (µm)Pore Size

(Å)


(g/mol) (PS) Part no.25 x 300 10 50 up to 2,000 PL1210-611525 x 300 10 100 up to 4,000 PL1210-612025 x 300 10 500 500-30,000 PL1210-612525 x 300 10 103 500-60,000 PL1210-613025 x 300 10 104 10,000-600,000 PL1210-614025 x 300 10 105 60,000-2,000,000 PL1210-615025 x 300 10 106 600,000-10,000,000 PL1210-6160MIXED-B25 x 300

10 500-10,000,000 PL1210-6100

MIXED-D25 x 300

10 200-400,000 PL1210-6104

Prep guard25 x 25

PL1210-1120

Plgel Preparative Columns


Columns for Special GPC/SEC ApplicationsEnviroPrep• High sample loading ensures effective trace analysis• Simple clean-up procedure saves sample preparation costs• Optimized particle size distribution provides high resolution

EnviroPrep columns permit a simple, one stage clean-up as part of a methodology to determine pesticides in many organic matrices. The higher molecular weight fractions such as lipids, polymers, natural resins and dispersed high molecular weight components are easily eliminated in the GPC analysis.

Preparative GPC for soil extract clean-up is described in EPA Method 3640A using 300 x 25 mm and 150 x 25 mm columns to give higher sample loading and fraction yields, which is particularly useful for low levels of pollutants. Low pore size EnviroPrep columns are ideal for this method. The columns have 10 µm particles with 100Å pore sizes for high resolution, with an exclusion limit of 4000 g/mol. The preparative columns offer good resolution and high loading through optimization of the particle size distribution.

EnviroPrepSize (mm) Part no.21.2 x 150 PL1E10-3120EPA25 x 150 PL1210-3120EPA21.2 x 300 PL1E10-6120EPA25 x 300 PL1210-6120EPA

Columns for sample clean-upColumn: EnviroPrep

Pl1210-6120EPa25 x 300 mm

Column: EnviroPrepPl1210-3120EPa25 x 150 mm

Mobile Phase: DCM

Flow Rate: 10 mL/min



1

2

3

4 5

0VLC0017

min 22

1. Corn oil, 25,000 mg/L2. Bis(2-ethylhexyl) phthalate, 1,000 mg/L3. Methoxychlor, 200 mg/L4. Perylene, 20 mg/L5. Sulfur, 80 mg/L

508


Plgel olexis• Optimized design for polyolefin analysis• High temperature capability• High resolution with no damage from sample shear provides clean separations

PLgel Olexis is designed for the analysis of very high molecular weight polymers, specifically polyolefins. The column resolves up to 100,000,000 g/mol (polystyrene in THF), and is packed with 13 µm particles tooptimize efficiency and resolution without the risk of sample shear degradation during analysis. The packingof PLgel Olexis has the mechanical stability and robustness expected from a PLgel column, and so it is ableto operate up to 220 °C for the analysis of highly crystalline materials.

Plgel olexisdescription Size (mm) Part no.PLgel Olexis 7.5 x 300 PL1110-6400PLgel Olexis guard 7.5 x 50 PL1110-1400

30

1

VLC0018Log M

dw/d

log

M

7

Plgel olexis reveals true modalities across the range of polyolefinsColumn: 3 x Plgel olexis

Pl1110-64007.5 x 300 mm

Mobile Phase: Trichlorobenzene + 0.0125% BHT



Temperature: 160 °C

Detector: PL-GPC 220 (RI)


Pl hFiPgel• Optimized separation range delivers high performance with no artifacts• Highly durable packing prolongs column lifetime• Low operating pressure reduces system wear and unnecessary downtimes

Hexafluoroisopropanol (HFIP) is used as a solvent in GPC for the analysis of important industrial polymerssuch as polyesters, polyamides and polylactide/glycolide copolymers. For greatly improved performance inextremely polar solvents such as HFIP and trifluoroethanol, we have developed novel "multipore"technology to produce PL HFIPgel, a PS/DVB packing featuring a monodisperse particle size, high porevolume, and high resolution.

Using PL HFIPgel avoids issues associated with conventional packings and HFIP, such as excessivecurvature of calibration curves, dislocations/shoulders on peaks for polydisperse samples, and poorresolution in the low MW region.

Column efficiency is guaranteed > 30,000 p/m and the columns are very durable, with a maximumoperating pressure of 145 bar (2030 psi). They are packed and tested in methanol but shipped ready-to-use in HFIP.

PL HFIPgel columns with 7.5 mm id normally operate at 1 mL/min. However, the 4.6 mm id columns run at0.3 mL/min, providing a 70% reduction in solvent consumption with consequent savings in the cost ofbuying and disposing of solvents.

MW range for PL HFIPgel columns is 2,000,000 g/mol (PMMA in THF).


Pl hFiPgeldescription Size (mm) Part no.PL HFIPgel 4.6 x 250 PL1514-5900HFIPPL HFIPgel 7.5 x 300 PL1114-6900HFIPPL HFIPgel guard 7.5 x 50 PL1114-1900HFIPPL HFIPgel guard 4.6 x 50 PL1514-1900HFIP

5VLC0019

min 22

nylon 66

nylon 6

PBT

PolyamidesColumn: 2 x Pl hFiPgel

Pl1114-6900hFiP7.5 x 300 mm

Mobile Phase: HFIP + 20mM NaTFAc


Temperature: 40 °C


510


Pl rapide• Analysis in less than ten minutes saves time• Significantly increased sample throughput improves efficiency• Reduced solvent consumption and disposal costs save money• Available in L, M, and H versions for low, medium, and high molecular weights; available in F version

for flow injection analysis

Rapid GPC is an excellent tool for screening polymer MWD for trend analysis. Short PL Rapide columnsreduce analysis times while maintaining the excellent solvent compatibility and mechanical stability of allGPC columns from Agilent.

PL Rapide columns are ideal for high speed applications such as high throughput screening, processmonitoring, or tracking changes in MW distributions, where time is the most critical factor in the analysis.Packed with high quality gels, these columns cover the complete spectrum of molecular weights and areavailable for the analysis of both organic and water soluble polymers. Key features include high porevolume, high resolution packing materials, no special system requirements, choice of molecular weightresolving range, wide solvent compatibility, and excellent mechanical stability.



Pl rapide

description Size (mm)mw range

(g/mol)Guaranteed

Efficiency (p/m) Part no.PL Rapide H 7.5 x 150 500-10,000,000 > 35,000 PL1113-3100

10 x 100 PL1013-2100PL Rapide M 7.5 x 150 200-2,000,000 > 60,000 PL1113-3500

10 x 100 PL1013-2500PL Rapide L 7.5 x 150 200-400,000 > 80,000 PL1113-3300

10 x 100 PL1013-2300PL Rapide F 7.5 x 150 up to 4,500 > 55,000 PL1113-3120

10 x 100 up to 4,500 > 40,000 PL1013-2120PL Rapide Aqua H 7.5 x 150 100-10,000,000 > 35,000 PL1149-3800

10 x 100 PL1049-2800PL Rapide Aqua L 7.5 x 150 100-30,000 > 35,000 PL1120-3830

10 x 100 PL1020-2830

resin analysis by rapid GPCColumn: Pl rapide l

Pl1013-230010 x 100 mm

Sample: Epoxy resin

Mobile Phase: THF

Flow Rate: 1.0 , 2.0 and 3.0 mL/min


0VLC0020

min 6

1.0 ml/min

2.0 ml/min

3.0 ml/min

512


PolarGel• Medium polarity surface and high mechanical stability• Operate in a wide range of solvents and solvent combinations• Available in two resolving ranges, PolarGel-L and PolarGel-M

With polar polymers, highly polar groups can lead to non-specific interactions and secondary separationmechanisms when using polar solvents and traditional non-polar styrene/divinylbenzene columns. Additives and/or column conditioning are normally required to reduce these interactions. PolarGel has no need for these interventions, and also avoids the interactions and secondary effects that producechromatogram distortions.

These PolarGel "mixed bed" columns have a medium polarity surface and high mechanical stability. They arecapable of operating in a wide range of solvents and solvent combinations, greatly enhancing your ability toanalyze polar polymers that are not necessarily water soluble. PolarGel is available in two resolving rangesto meet your precise requirements.

PolarGel

description Size (mm)mw range(g/mol) (PEG/PEo) Part no.

PolarGel-L 7.5 x 300 Up to 30,000 PL1117-6830PolarGel-L guard 7.5 x 50 PL1117-1830PolarGel-L repair gel PL1417-0830PolarGel-M 7.5 x 300 Up to 2,000,000 PL1117-6800PolarGel-M guard 7.5 x 50 PL1117-1800PolarGel-M repair gel PL1417-0800

The PolarGel range is ideal for use with polar solvents, such as dimethyl formamide (DMF) and dimethylsulfoxide (DMSO), and for solvent combinations such as tetrahydrofuran with water. These eluents are veryuseful in GPC/SEC to separate polar materials, such as polar resins, modified polysaccharides or complexpolar polymers that are difficult to analyze in traditional SEC solvents, such as tetrahydrofuran alone.PolarGel-L is used for low molecular weight polar polymers and PolarGel-M for high MW polar polymers.



Two samples of melamine resin analyzed by PolarGel-lColumn: 2 x PolarGel-l, 300 x 7.5 mm

Pl1117-6830Mobile Phase: Dimethyl acetamide + 0.1% LiBr



Detector: Agilent PL-GPC 220 (RI)

0VLC0021

min 22

0VLC0022

min 22

Excellent separation of two phenolformaldehyde resins with PolarGel-mColumn: 2 x PolarGel-m, 300 x 7.5 mm

Pl1117-6800Mobile Phase: 0.2% (w/v) DMF & 0.1% LiBr to reduce sample

aggregation




514


PlusPoreThe PlusPore range has an increased pore volume that provides high resolution for specific applications. The high stability media permits the use of a wide range of organic solvents with accuracy and precision so that there is no distortion of the MW distribution shape.

The PlusPore series of columns has been specifically designed for high resolution GPC, and represents the very latest in GPC column technology. These novel packing materials are based on the industrystandard, highly cross-linked polystyrene/divinylbenzene (PS/DVB), for the widest applicability and solventcompatibility. Each is made using a novel polymerization process to produce particles that exhibit a specific,controlled pore structure for optimum GPC performance. Typical applications include resins, condensationpolymers, prepolymers, and oligomers.

For high resolution polymer analysis, the PolyPore, ResiPore, MesoPore, and OligoPore columns of thePlusPore product series exhibit a wide pore size distribution with near linear calibration curves covering anextended molecular weight range. These so-called "multipore" structures have increased pore volumecompared to regular PS/DVB packing materials. This results in very high resolution GPC columns designedfor specific application areas. The highly cross-linked porous particles provide excellent chemical andphysical stability and permit easy transfer across the full range of organic solvents with little change in theshape of the calibration curve or the efficiency of the columns. As this multipore column technology doesnot require the combination of individual pore size packing materials, the result is high accuracy andprecision without any artifacts in the shape of the molecular weight distribution.



PlusPore calibration curves

PlusPore Selection Guide

Columnmw range

(g/mol) (PS)nominal

Particle Size (µm)Typical Efficiency

(p/m) recommended Calibrants Frit Porosity (µm)PolyPore 200-2,000,000 5 > 60,000 EasiCal PS-1or EasiVial PS-H 2ResiPore 200-400,000 3 > 80,000 EasiCal PS-2 or EasiVial PS-M 2MesoPore up to 25,000 3 > 80,000 Polystyrene S-L-10 Kit 2OligoPore up to 4,500 6 > 55,000 Polystyrene S-L2-10 Kit 2

VLC0023

4

2

6.5

10

Key

PolyPore

ResiPore

MesoPore

OligoPore

Log M

W

Retention time/min

516


PolyPore• Routine polymer analysis with very high resolution• Wide operating range simplifies column choice• Low particle size extracts maximum information from the analyte

PolyPore columns have been specifically developed to give unrivaled resolution for the analysis of polymerswith broad molecular weight distributions. With a wide operating range covering many decades ofmolecular weight, PolyPore columns combine a 5 µm particle size with extremely high pore volume to givethe highest possible resolution, ensuring the most detailed information possible from your analysis.

PolyPoredescription Size (mm) Part no.PolyPore 7.5 x 300 PL1113-6500PolyPore guard 7.5 x 50 PL1113-1500



5VLC0024

20

PolyPore (a)

Retention time/min

individual Pore Size Columns (B & C)

Polymethylmethacrylate in dmFColumn: 2 x PolyPore

Pl1113-65007.5 x 300 mm

Sample: Commercial PMMA

Mobile Phase: DMF + 0.1% LiBr


Temperature: 80 °C



0VLC0025

24Retention time/min

Comparison of PolyPore with conventionalindividual pore size GPC columnsColumn a: 2 x PolyPore

Pl1113-65007.5 x 300 mm

Column B: Plgel 103Å7.5 x 300 mm, 5 µm

Column C: Plgel 105Å7.5 x 300 mm, 5 µm

Sample: High MW Resin

Mobile Phase: THF


Injection Volume 100 µL


518


resiPore• Efficient separation of complex molecular weight distributions• Reveals oligomer content to provide a true representation of the sample• High pore volume extracts maximum information from the analyte

ResiPore columns are the ideal choice for the analysis of resins and condensation polymers with complexmolecular weight distributions that include oligomer content. By combining a 3 µm particle size and highpore volume, high efficiency ResiPore columns offer maximum resolution of these intermediate molecularweight polymers.

resiPoredescription Size (mm) Part no.ResiPore 7.5 x 300 PL1113-6300ResiPore guard 7.5 x 50 PL1113-1300



5VLC0026


5VLC0027


alkyd resinColumn: 2 x resiPore

Pl1113-63007.5 x 300 mm

Mobile Phase: THF




PolyesterColumn: 2 x resiPore

Pl1113-63007.5 x 300 mm

Mobile Phase: THF




520


mesoPore• Full solvent compatibility with no detrimental effect on efficiency• Low particle size extracts maximum information from the analyte• No MWD dislocations so the distribution is an accurate representation of the sample

MesoPore columns have been specifically designed to provide optimum results in the analysis ofprepolymers, i.e. polymeric materials with a large oligomeric component. By combining a 3 µm particle sizewith high pore volume, MesoPore columns give the highest resolution separations for the analysis of lowmolecular weight polymers, such as prepolymers, resins, polyols, and siloxanes.

mesoPoredescription Size (mm) Part no.MesoPore 7.5 x 300 PL1113-6325MesoPore guard 7.5 x 50 PL1113-1325

5VLC0028


5VLC0029


PolyurethanesColumn: 2 x mesoPore

Pl1113-63257.5 x 300 mm

Mobile Phase: THF




PolyesterimideColumn: 2 x mesoPore

Pl1113-63257.5 x 300 mm

Mobile Phase: THF






oligoPore• Near linear calibration curve for best accuracy and precision• Very stable media allows for a wide choice of solvents• Isolation of individual fractions reveals more information from whole samples

OligoPore columns have been developed from an innovative new media that exhibits significantly increasedpore volumes compared to conventional low pore size GPC columns. The outcome is higher resolution in theoligomeric region. The 300 x 25 mm preparative column offers high resolution at greatly increased loadingfor effective isolation of individual components. Oligomer fractions collected from the OligoPore preparativecolumn can then be re-injected on analytical columns to check for the purity of the fractions and forcomparison with the whole sample.

oligoPoredescription Size (mm) Part no.OligoPore 25 x 300 PL1213-6520OligoPore 7.5 x 300 PL1113-6520OligoPore guard 7.5 x 50 PL1113-1320

522


10

F1

F2

F3

F4

F5

F6

F7

F8

F9

VLC0030

20

whole polymer

Retention time/min

5VLC0031

20

5 20Retention time/min

Retention time/min

analysis of low molecular weight polystyreneand oligomer fractions collected from oligoPore preparative columnsColumn: 2 x oligoPore

Pl1113-65207.5 x 300 mm

Mobile Phase: THF


Detector: UV

analytical separation of low molecular weight polystyreneColumn: 2 x oligoPore

Pl1213-65207.5 x 300 mm

Mobile Phase: THF


Loading: 0.2%, 100 mL

Detector: UV

Preparative separation of low molecular weight polystyreneColumn: 2 x oligoPore

Pl1213-652025 x 300 mm

Mobile Phase: THF


Loading: 2.0%, 2 mL

Detector: UV



Aqueous SEC of PolymersPl aquagel-oh SECAqueous size exclusion chromatography (SEC) is widely used for the determination of molecular weightdistributions of a variety of synthetic and naturally occurring water-soluble polymers, and separations ofoligomers and small molecules. The requirement to eliminate ionic and hydrophobic effects makes aqueousSEC very demanding.

The PL aquagel-OH series provides a chemically and physically stable matrix for reliable aqueous SECseparations. The columns are packed with macroporous copolymer beads with an extremely hydrophilicpolyhydroxyl functionality. The "neutral" surface and the capability to operate across a wide range of eluentconditions provide for high performance analyses of compounds with neutral, ionic, and hydrophobicmoieties, alone or in combination. PL aquagel-OH is available for analytical and preparative applications.

Optimizing Conditions for Aqueous SEC with PL aquagel-OH ColumnsDue to the complex nature of water-soluble polymers, it is often necessary to modify the eluent in order to avoid sample-to-sample and sample-to-column interactions which can result in poor aqueous SECseparations. The excellent stability of the PL aquagel-OH packing material allows the eluent to be tailored to suit the polymer, while retaining the high column efficiency. For ionic interactions, the eluent can be modified by the addition of salt and/or the adjustment of pH. For water soluble polymers with ahydrophobic character, only the addition of a weak organic solvent (methanol) is required to inhibithydrophobic interactions.

524


Guide to eluent selection for Pl aquagel-oh applications

water soluble polymer

Polymer Chemistry Neutral Anionic Cationic

Suggested Eluent Pure Water0.1-0.3 M NaNO3

pH 7-90.01 M NaH2PO4

0.2-0.8 M NaNO3pH 2-7

0.01 M NaH2PO4

hydrophobic Polymers Addition of up to 50% methanol

Pl aquagel-oh Column Selection Guide

Sample Type Typical applications recommended Column SetsLow MW polymers and oligomers Surfactants, oligosaccharides, PEGs,

lignosulfonates, polyacrylates2 or 3, 30, 20PL aquagel-OH 8 µm, orPL aquagel-OH 20 5 µm, orPL aquagel-OH MIXED-M 8 µm

Polydisperse synthetic or naturally occurring polymers

Polysaccharides, PVA, cellulose derivatives, PEO, polyacrylic acid

2 or 3PL aquagel-OH MIXED-H 8 µm, orPL aquagel-OH 60/50/40 8 µm

Very high MW polymers Polyacrylamides, hyaluronic acids, CMC, starches, gums




• Highly stable matrix ensures reliable separations, even with modified eluents• MIXED columns cover a wide range of molecular weights, simplifying column selection• Highly versatile for neutral, polar, anionic and cationic samples

The PL aquagel-OH analytical series has a pH range of 2-10, compatibility with organic solvent (up to 50% methanol), mechanical stability up to 140 bar (2030 psi) and low column operating pressures.

Pl aquagel-oh analytical


(g/mol) (PEG/PEo)


(p/m) Part no.PL aquagel-OH 20 5 µm 7.5 x 300 100-20,000 > 5,000 PL1120-6520PL aquagel-OH 20 8 µm 7.5 x 300 100-20,000 > 35,000 PL1149-6820PL aquagel-OH 30 8 µm 7.5 x 300 100-30,000 > 35,000 PL1120-6830PL aquagel-OH 40 8 µm 7.5 x 300 10,000-200,000 > 35,000 PL1149-6840PL aquagel-OH 40 15 µm 7.5 x 300 10,000-200,000 > 15,000 PL1149-6240PL aquagel-OH 50 8 µm 7.5 x 300 50,000-1,000,000 > 35,000 PL1149-6850PL aquagel-OH 50 15 µm 7.5 x 300 50,000-1,000,000 > 15,000 PL1149-6250PL aquagel-OH 60 8 µm 7.5 x 300 200,000-> 10,000,000 > 35,000 PL1149-6860PL aquagel-OH 60 15 µm 7.5 x 300 200,000-> 10,000,000 > 15,000 PL1149-6260PL aquagel-OH MIXED-H 8 µm 7.5 x 300 100-10,000,000 > 35,000 PL1149-6800PL aquagel-OH MIXED-M 8 µm 7.5 x 300 Up to 600,000 > 35,000 PL1149-6801PL aquagel-OH 10 µm guard 25 x 25 PL1249-1120PL aquagel-OH 5 µm guard 7.5 x 50 PL1149-1530PL aquagel-OH 8 µm guard 7.5 x 50 PL1149-1840

Buffers in a stored column maycrystallize and cause damage.Flush the column with watercontaining a small amount ofsodium azide to preventbiological growth.

TiPS & ToolS

Pl aquagel-oh analytical

526


Polyvinyl alcoholColumn: 3 x Pl aquagel-oh miXEd-h 8µm

Pl1149-68007.5 x 300 mm

Mobile Phase: 0.2 M NaNO3, 0.01 M NaH2PO4, pH 7



10VLC0032


heparinColumn: 2 x Pl aquagel-oh 30 8 µm

Pl1120-68307.5 x 300 mm




5VLC0033


1.0

dw/L

og M

Cum

.Ht

0.0

8.0

0.0

1.0

VLC0035Log M 3.5

5

dw/d

log

M0

1

VLC0034Log M 7

5 min 18



hyaluronic acidColumn: Pl aquagel-oh 60 15 µm

Pl1149-62607.5 x 300 mm

andPl aquagel-oh 40 15 µmPl1149-62407.5 x 300 mm




Chromatogram

Mw 1,800,00 g/mol

differences in composition of two alkylnaphthalene sulfonatesColumn: 2 x Pl aquagel-oh 20 5µm

Pl1120-65207.5 x 300 mm

Mobile Phase: 0.25 M ammonium formate in water




528


• Up to 10 times scale-up maximizes yield• High loading maximizes sample throughput• Carefully chosen particle size provides optimum resolution

Preparative SEC is used for the fractionation of a wide variety of water-soluble samples based on their sizein solution. The technique is applied to the fractionation of disperse polymers or to isolate components in apolymer formulation.

Preparative PL aquagel-OH columns and associated guard columns enable rapid and convenient scale-upfrom analytical separations. The 25 mm id prep column offers at least a 10 times scale-up in loading fromthe 7.5 mm id analytical columns. Typically, a 10 mL/min flow rate results in a separation time of tenminutes with a 300 mm column. The columns are packed with the same robust macroporous particles asthe analytical column range. The 8 µm particle size provides optimum resolution and loading characteristicswith column efficiency > 20,000 plates/m.

Pl aquagel-oh Preparative


(g/mol) (PEG/PEo) Part no.PL aquagel-OH 30 8 µm 25 x 300 100-30,000 PL1220-6130PL aquagel-OH 40 8 µm 25 x 300 10,000-200,000 PL1249-6140PL aquagel-OH 50 8 µm 25 x 300 50,000-1,000,000 PL1249-6150PL aquagel-OH MIXED 8 µm 25 x 300 100-10,000,000 PL1249-6100PL aquagel-OH 10 µm guard 25 x 25 PL1249-1120

0VLC0036


Pl aquagel-oh Preparative

Polyvinyl alcoholColumn: Pl aquagel-oh 40 8 µm

Pl1249-614025 x 300 mm



Loading: 10 mg/mL, 2 mL




GPC Column accessoriesdescription unit Part no.Frit removal tool for threaded columns only 1/pk PL1310-00012 µm frit kit for threaded columns, 7.5 mm id 5/pk PL1310-00025 µm frit kit for threaded columns, 7.5 mm id 5/pk PL1310-001210 µm frit kit for threaded columns, 7.5 mm id 5/pk PL1310-0036PLgel column repair gel, 10 µm 1/pk PL1410-0101PLgel column repair gel, 5 µm 1/pk PL1410-0501Column connecting nuts, 1/16 in tube 5/pk PL1310-0007Tubing ferrules, 1/16 in tube 5/pk PL1310-0008Connecting tubing, 10 cm length, 0.01 in id 10/pk PL1310-0048LDV intercolumn stainless steel connector 1/pk PL1310-0005PLgel column repair gel, 3 µm 1/pk PL1410-0301PLgel Olexis column repair gel 1/pk PL1410-0200

530


Polymer Standards for GPC/SECPolymer standards from Agilent are the ideal reference materials for generating accurate, reliable GPC/SECcolumn calibrations, with the assurance of the ISO 9001:2000 quality standard. Additional applications forour highly characterized homopolymers exhibiting unique characteristics are used as model polymers forresearch and analytical method development.

Agilent manufactures the highest quality polymer standards with extremely narrow polydispersity and thewidest molecular weight range commercially available. These quality polymer standards are supplied withextensive characterization data utilizing a variety of independent techniques (e.g. light scattering andviscometry) and high performance GPC to verify polydispersity and assign that all important peak molecularweight (Mp).

Our comprehensive range of EasiVial, EasiCal, and traditional calibration kits has been specifically designedto cover all molecular weight ranges for organic and aqueous GPC/SEC applications. We provide you withthe widest choice to maximize your specific characterization needs. In addition, we supply other polymers asindividual molecular weights, and broad distribution polymers for system validation or broad standardcalibration procedures.



Calibration KitsAgilent offers a wide range of polymer standards kits for conventional GPC/SEC column calibration or forcalibrating light scattering and viscometry detectors. The kits are in boxed sets of ten different polymerstandards covering a particular molecular weight range, to be used with organic and aqueous, mediumpolarity, and polar solvents. Every individual polymer has its own Certificate of Analysis of the analyticalconditions and values, such as Mp needed for constructing a calibration plot. The polymers are chosen togive equidistant calibration points on a logarithmic MW scale, providing a more uniform calibration curve.

individual Polymer molecular weightsWe design our individual standards to have the narrowest molecular weight distribution commerciallyavailable. Additionally, they cover the widest molecular weight range, from 162-15 million MW. The currentpolystyrene nominal molecular weight of 15 million MW has a polydispersity ≤1.10. These standards aregenerally available in 1, 5 and 10 g quantities, and each comes with its own Certificate of Analysis detailinganalysis conditions and relevant data.

GPC/SEC Standards Selection Guide

Polymer Typeindividual

mwCalibration

Kits EasiCal EasiVial Type of GPC/SECPolystyrene 3 3 3 3 OrganicPolymethylmethacrylate 3 3 3 OrganicPolyethylene glycol (PEG) 3 3 3 Organic/AqueousPolyethylene oxide (PEO) 3 3 3 Organic/AqueousPullulan polysaccharide 3 3 Organic/AqueousPolyacrylic acid Na salt 3 3 Aqueous

532


EasiVial• Eliminates tedious weighing procedures to improve calibration accuracy• Reduces solvent dispensing to limit risks associated with handling solvents• For conventional and multi detector GPC to maximize applicability

For organic and aqueous GPC/SEC column calibration, this premier product is the quickest and mostconvenient method to deliver an accurate 12-point column calibration.

The key to achieving baseline separation from polymer mixtures, and therefore eliminating doubt and errors,is in selecting only the narrowest polydispersity polymers. This is where Agilent polymer standards excel anddeliver, as shown in the chromatograms.

The EasiVial standards kit is a pre-prepared, time saving product for rapid and reliable GPC columncalibration. EasiVial kits contain three vials, each with a mixture of four accurately pre-weighed polymerstandards, providing a 12-point GPC calibration in just three injections. The mass of each polymer in the vialis accurately known, so that upon addition of a fixed volume of eluent, the solution is prepared at a preciseconcentration. EasiVial is ideal for both conventional and multi detector GPC calibration. Simply prepare andmanually inject, or transfer to autosampler vials, or place directly into a compatible autosampler.

Every EasiVial kit contains 30 vials (ten of each type) that are color-coded for easy identification and areavailable in 4 or 2 mL vials making them suitable for most autosamplers. The kits are available forpolystyrene (PS), polymethylmethacrylate (PMMA), polyethylene glycol/oxide (PEG/PEO) and polyethyleneglycol (PEG). For added value, a Tri-Pack (90 vials) is offered, extending reproducibility.

15

LogM

1.0e2

1.0e7

VLC0044

29



Polystyrene calibration generated with EasiVials

Retention time/min

1. 6,035,0002. 483,0003. 19,7204. 1,2605. 3,053,0006. 84,9007. 8,4508. 5809. 915,000

10. 60,45011. 3,37012. 162

10

10 11 12

78

9

4

5

6

1

2

3

VLC0037min 33

EasiVial PS-hColumn: 3 x Plgel 10 µm miXEd-B

Pl1110-61007.5 x 300 mm

Mobile Phase: THF


Temperature: 40 °C


534


Specifications

EasiVial Color EasiVial PS-h EasiVial PS-m EasiVial PS-l EasiVial Pm EasiVial PEG/PEo EasiVial PEGnominal mp (g/mol)

Red 1,300 780 580 2,000 600 28220,000 6,000 3,000 30,000 12,000 1,000

500,000 50,000 10,000 300,000 125,000 6,0006,000,000 400,000 40,000 2,000,000 1,200,000 35,000

Yellow 580 370 370 1,000 200 1948,500 2,500 2,000 13,000 4,000 600

185,000 25,000 6,000 150,000 60,000 3,7503,000,000 200,0001 25,000 800,000 1,000,000 21,000

Green 162 162 162 600 100 1063,400 1,500 1,000 5,700 1,500 420

60,000 11,000 4,000 80,000 25,000 2,000900,000 100,000 16,000 470,000 460,000 12,000

description KeyPS: PolystyrenePM: PolymethylmethacrylatePEG/PEO: Polyethylene Glycol/OxideH: HighM: MediumL: Low



EasiVial Pre-weighed Calibration Kits

descriptionrange of nominal mp

(g/mol)Vial Volume

(ml) unit Part no.EasiVial PEG/PEO 100-1,200,000 2 30/pk PL2080-0201EasiVial PEG/PEO 100-1,200,000 4 30/pk PL2080-0200EasiVial PEG 106-35,000 2 30/pk PL2070-0201EasiVial PEG 106-35,000 4 30/pk PL2070-0200EasiVial PM 600-2,000,000 2 30/pk PL2020-0201EasiVial PM 600-2,000,000 4 30/pk PL2020-0200EasiVial PS-H 162-6,000,000 2 30/pk PL2010-0201EasiVial PS-H 162-6,000,000 4 30/pk PL2010-0200EasiVial PS-M 162-400,000 2 30/pk PL2010-0301EasiVial PS-M 162-400,000 4 30/pk PL2010-0300EasiVial PS-L 162-40,000 2 30/pk PL2010-0401EasiVial PS-L 162-40,000 4 30/pk PL2010-0400PEG/PEO Tri-Pack 2 90/pk PL2080-0202PEG/PEO Tri-Pack 4 90/pk PL2080-0203PEG Tri-Pack 2 90/pk PL2070-0202PEG Tri-Pack 4 90/pk PL2070-0203PMMA Tri-Pack 2 90/pk PL2020-0202PMMA Tri-Pack 4 90/pk PL2020-0203PS-H Tri-Pack 2 90/pk PL2010-0202PS-H Tri-Pack 4 90/pk PL2010-0203PS-L Tri-Pack 2 90/pk PL2010-0402PS-L Tri-Pack 4 90/pk PL2010-0403

536


EasiCal• Easy three-step process with no fuss• Cost-effective format saves money• Only two injections for improved productivity

The EasiCal system for organic solvents consists of two different combs, each with ten detachable spatulas,supporting a mixture of five polymer standards. The thin film of polymer (approximately 5 mg) on the tip ofthe PTFE spatulas rapidly dissolves when immersed in eluent to provide two GPC/SEC calibration solutions.A single pack provides ten spatulas of each type, with MWs selected to provide equidistant calibrationpoints for greater accuracy.

EasiCal Pre-prepared Polystyrene Kitsdescription range of nominal mp (g/mol) unit Part no.Polystyrene PS-1 580-7,500,000 1/pk PL2010-0501

5/pk PL2010-0505Polystyrene PS-2 580-400,000 1/pk PL2010-0601

5/pk PL2010-0605

5 30

5 30

13

Log

MW

3

7

VLC0038

25

Column calibration for GPC/SEC is as easy as 1, 2, 3...

3. Generate a 10-point calibration

2. Chromatograph each solution; only two injections required

1. Place one spatula of each type into appropriate volume of solvent.

Retention time/min



Polystyrene• Compatible with most organic solvents• Certificate of Analysis meets international protocols• Calibration capability for virtually all applications

Polystyrene standards are the first choice for many organic solvents, either for conventional GPC columncalibration or for calibrating light scattering and viscosity detectors. Our organic polymers cover a rangefrom 162-15 million MW, with MWs selected to provide equidistant calibration points for greater accuracy.Every kit contains 0.5 g of ten different molecular weight standards.

Calibration Kits, (all Kits 10 x 0.5 g)S-h-10Part no.Pl2010-0103

S-h2-10Part no.Pl2010-0104

S-m-10Part no.Pl2010-0100

S-m2-10Part no.Pl2010-0102

S-l-10Part no.Pl2010-0101

S-l2-10Part no.Pl2010-0105

Constituent Polymer nominal mp (g/mol)300,000 1,000 580 580 162 162460,000 3,000 1,450 1,400 580 370700,000 8,600 4,000 2,400 900 5801,100,000 25,000 10,000 4,750 1,400 8001,700,000 73,000 27,000 9,500 2,200 1,0002,600,000 210,000 66,000 19,000 3,400 1,5004,000,000 600,000 180,000 38,000 5,100 1,9006,200,000 1,780,000 460,000 75,000 8,100 2,5009,500,000 5,000,000 1,190,000 150,000 12,800 3,20015,000,000 15,000,000 3,000,000 300,000 20,000 4,500

description KeyH: HighM: MediumL: Low

538


individual Polymer molecular weights

Polymer nominal mp (g/mol) nominal mw/mn1 gPart no.

5 gPart no.

10 gPart no.

162 1.00 PL2012-1001 PL2012-1005 PL2012-1010370 1.11 PL2012-0001 PL2012-0005 PL2012-0010580 1.11 PL2012-2001 PL2012-2005 PL2012-20101,000 1.09 PL2012-3001 PL2012-3005 PL2012-30101,300 1.07 PL2012-4001 PL2012-4005 PL2012-40102,000 1.05 PL2012-5001 PL2012-5005 PL2012-50103,000 1.04 PL2012-6001 PL2012-6005 PL2012-60105,000 1.03 PL2012-7001 PL2012-7005 PL2012-70107,000 1.04 PL2012-8001 PL2012-8005 PL2012-801010,000 1.02 PL2012-9001 PL2012-9005 PL2012-901020,000 1.02 PL2013-1001 PL2013-1005 PL2013-101030,000 1.02 PL2013-2001 PL2013-2005 PL2013-201050,000 1.03 PL2013-3001 PL2013-3005 PL2013-301070,000 1.03 PL2013-4001 PL2013-4005 PL2013-4010100,000 1.02 PL2013-5001 PL2013-5005 PL2013-5010130,000 1.01 PL2013-6001 PL2013-6005 PL2013-6010200,000 1.05 PL2013-7001 PL2013-7005 PL2013-7010300,000 1.03 PL2013-8001 PL2013-8005 PL2013-8010500,000 1.03 PL2013-9001 PL2013-9005 PL2013-9010700,000 1.03 PL2014-0001 PL2014-0005 PL2014-00101,000,000 1.05 PL2014-1001 PL2014-1005 PL2014-10101,500,000 1.04 PL2014-2001 PL2014-2005 PL2014-20102,000,000 1.04 PL2014-3001 PL2014-3005 PL2014-30102,500,000 1.05 PL2014-4001 PL2014-4005 PL2014-40104,000,000 1.04 PL2014-6001 PL2014-6005 PL2014-60107,000,000 1.04 PL2014-7001 PL2014-7005 PL2014-701010,000,000 1.06 PL2014-8001 PL2014-8005 PL2014-801015,000,000 1.06 PL2014-9001 PL2014-9005 PL2014-9010

Polystyrene standardsColumn: 2 x oligoPore

Pl1113-65207.5 x 300 mm

Mobile Phase: THF



0

1,270

580

VLC0039

min 20



Polymethylmethacrylate• Many solvent options increase applicability• Stringent quality control improves performance• Proprietary manufacturing methods ensure consistent supply

Polymethylmethacrylate (PMMA) standards are extremely versatile as they can be used for organic GPC with a wide range of medium polarity eluents, such as tetrahydrofuran, toluene, methyl ethyl ketone,and ethyl acetate. They also work well with more polar organic eluents, for example dimethylformamide,dimethylacetamide, and hexafluoroisopropanol. The MWs are selected to provide equidistant calibrationpoints for greater accuracy, covering from 500-1.5 million MW. Every kit contains 0.5 g of ten differentmolecular weight standards.

Calibration Kits, (all Kits 10 x 0.5 g)m-l-10Part no.Pl2010-0100

m-m-10Part no.Pl2020-0101

Constituent Polymer nominal mp (g/mol)600 1,000840 2,2001,400 5,0002,350 11,2003,900 25,5006,400 58,00010,800 130,00018,000 290,00030,000 660,00050,000 1,500,000

description KeyM: MediumL: Low

540




5 gPart no.

10 gPart no.

500 1.19 PL2022-2001 PL2022-2005 PL2022-20101,000 1.26 PL2022-3001 PL2022-3005 PL2022-30102,000 1.08 PL2022-5001 PL2022-5005 PL2022-50103,000 1.08 PL2022-6001 PL2022-6005 PL2022-60105,000 1.09 PL2022-7001 PL2022-7005 PL2022-70107,000 1.08 PL2022-8001 PL2022-8005 PL2022-801010,000 1.03 PL2022-9001 PL2022-9005 PL2022-901013,000 1.03 PL2023-0001 PL2023-0005 PL2023-001020,000 1.03 PL2023-1001 PL2023-1005 PL2023-101030,000 1.02 PL2023-2001 PL2023-2005 PL2023-201050,000 1.02 PL2023-3001 PL2023-3005 PL2023-301070,000 1.02 PL2023-4001 PL2023-4005 PL2023-4010100,000 1.02 PL2023-5001 PL2023-5005 PL2023-5010130,000 1.05 PL2023-6001 PL2023-6005 PL2023-6010200,000 1.02 PL2023-7001 PL2023-7005 PL2023-7010300,000 1.02 PL2023-8001 PL2023-8005 PL2023-8010500,000 1.06 PL2023-9001 PL2023-9005 PL2023-9010700,000 1.03 PL2024-0001 PL2024-0005 PL2024-00101,000,000 1.09 PL2024-1001 PL2024-1005 PL2024-10101,500,000 1.09 PL2024-2001 PL2024-2005 PL2024-2010

Polymethylmethacrylate standardsColumn: 2 x Pl hFiPgel

Pl1114-6900hFiP7.5 x 300 mm

Mobile Phase: HFIP + 20 mM NaTFAc


Temperature: 40 °C


5

1

2

3

4

5

VLC0040

22

1. 790,0002. 144,0003. 28,9004. 5,7205. 1,020

Retention time/min



Polyethylene Glycol/oxide• Simple-to-use kit form• Combines glycols and oxides to extend the MW range and cover more applications• MWs selected to provide equidistant calibration points for greater accuracy

These hydrophilic polymers are suitable for both aqueous SEC and organic GPC using the majority of polarorganic solvents. The oxides are available in high molecular weights, while the glycols cover the lowermolecular weight range. The two types are chemically similar so they can be used together across a widermolecular weight range, with aqueous and organic polymers from 106-1 million MW. Every kit contains 0.2 g or 0.5 g of ten different molecular weight standards.

Calibration KitsPEG-10 (10 x 0.5 g)Part no.Pl2070-0100

PEo-10 (10 x 0.2 g)Part no.Pl2080-0101

Constituent Polymer nominal mp (g/mol)106 20,000194 30,000400 50,000600 70,0001,000 100,0002,000 200,0004,000 300,0007,000 400,00013,000 700,00020,000 1,000,000

542




5 gPart no.

10 gPart no.

Polyethylene Glycol106 1.00 PL2070-1001 PL2070-1005 PL2070-1010194 1.00 PL2070-2001 PL2070-2005 PL2070-2010238 1.00 PL2071-2001 PL2071-2005 PL2071-2010282 1.00 PL2071-3001 PL2071-3005 PL2071-3010420 1.09 PL2070-3001 PL2070-3005 PL2070-3010600 1.06 PL2070-4001 PL2070-4005 PL2070-40101,000 1.04 PL2070-5001 PL2070-5005 PL2070-50101,500 1.04 PL2070-6001 PL2070-6005 PL2070-60104,000 1.03 PL2070-7001 PL2070-7005 PL2070-70107,000 1.04 PL2070-8001 PL2070-8005 PL2070-801010,000 1.05 PL2070-9001 PL2070-9005 PL2070-901013,000 1.07 PL2071-0001 PL2071-0005 PL2071-001020,000 1.07 PL2071-1001 PL2071-1005 PL2071-1010Polyethylene oxide20,000 1.05 PL2083-1001 PL2083-1005 PL2083-101030,000 1.07 PL2083-2001 PL2083-2005 PL2083-201050,000 1.05 PL2083-3001 PL2083-3005 PL2083-301070,000 1.05 PL2083-4001 PL2083-4005 PL2083-4010100,000 1.06 PL2083-5001 PL2083-5005 PL2083-5010130,000 1.07 PL2083-6001 PL2083-6005 PL2083-6010200,000 1.07 PL2083-7001 PL2083-7005 PL2083-7010300,000 1.07 PL2083-8001 PL2083-8005 PL2083-8010500,000 1.06 PL2083-9001 PL2083-9005 PL2083-9010700,000 1.07 PL2084-0001 PL2084-0005 PL2084-00101,000,000 1.12 PL2084-1001 PL2084-1005 PL2084-10101,500,000 1.13 PL2084-2001 PL2084-2005 PL2084-2010

1

1

2

3

4

5

VLC0041


1. 1,702,0002. 120,0003. 12,6004. 1,4705. 106

Polyethylene Glycol/oxide standardsColumn: Pl aquagel-oh miXEd-h 8 µm

Pl1149-68007.5 x 300 mm

Mobile Phase: Water





Polysaccharides• Comprehensive format provides full MW range in one handy kit• Also available as individual standards

The pullulan polysaccharides kit consists of several simple sugars with relatively narrow polydispersity linearmacromolecules of maltotriose units.

Calibration KitsSaC-10 (10 x 0.2 g)Part no.Pl2090-0100Constituent Polymer nominal mp (g/mol)1807385,00010,00020,00050,000100,000200,000400,000700,000

544


individual Polymer molecular weightsPolymer nominal mp (g/mol) unit Part no.1,500 0.2 g PL2091-20002,000 0.2 g PL2091-30003,000 0.2 g PL2091-40005,000 0.5 g PL2090-100020,000 0.5 g PL2090-300050,000 0.5 g PL2090-4000100,000 0.5 g PL2090-5000200,000 0.5 g PL2090-6000700,000 0.5 g PL2090-80001,660,000 0.2 g PL2091-1000

1. 788,0002. 212,0003. 47,3004. 11,8005. 667

Pullulan polysaccharide standardsColumn: 3 x Pl aquagel-oh miXEd-h 8 µm

Pl1149-68007.5 x 300 mm




8

1 23

4

5

VLC0042




Polyacrylic acid• Compatible with all aqueous columns for wide applicability• Aqueous polymers 1,000-2 million MW• Well-characterized Mp values ensure wide utility


Polymer nominal mp (g/mol)0.2 gPart no.

1 gPart no.

1,000 PL2142-3000 PL2142-30012,000 PL2142-50003,000 PL2142-6000 PL2142-60015,000 PL2142-7000 PL2142-70017,000 PL2142-8000 PL2142-800113,000 PL2143-0000 PL2143-010130,000 PL2143-2000 PL2143-200150,000 PL2143-3000 PL2143-300170,000 PL2143-4000 PL2143-4001100,000 PL2143-5000 PL2143-5001130,000 PL2143-6000 PL2143-6001200,000 PL2143-7000 PL2143-7001300,000 PL2143-8000 PL2143-8001500,000 PL2143-9000 PL2143-9001700,000 PL2144-0000 PL2144-01011,000,000 PL2144-1000 PL2144-10011,500,000 PL2144-2000 PL2144-20012,000,000 PL2144-3000 PL2144-3001

Calibration KitsPaa-10 (10 x 0.2 g)Part no.Pl2140-0100Constituent Polymer nominal mp (g/mol)1,0003,0007,00013,00030,00070,000100,000300,000700,0001,000,000

644

PRODUCT INDEX

Agilent SuppliesAutosamplersInjection Valves.........................................................61Kits..........................................................................66-67Loop Capillaries.........................................................64Maintenance Schedule ...........................................61Metering Device........................................................64Needles and Needle Seats...............................62-63Trays.............................................................................65

Bio-inert QuaternaryAutosampler ....................................................101-102Column Compartment ...........................................102Detectors ..................................................................102Fittings.......................................................................102Pumps .......................................................................101Valves ........................................................................102

Capillaries1200 and 1100 Prep LC Systems ..........................261220/1120 Infinity Series LC Systems ................331260 Bio-inert LC System.......................................301260/1200/1100 Infinity Series LC Systems.....231290 Infinity Series LC Systems ...........................241290 Valve Head..................................................25-27Loop .............................................................................32Miscellaneous .....................................................27-29PEEK Coated Fused Silica Capillaries –100 µL/min Flow ......................................................32PEEK Coated Fused Silica Capillaries –20 µL/min Flow.........................................................31PEEK Coated Fused Silica Capillaries for Nano LC................................................................31

Chip LC ........................................................................100Detectors80 nL and 500 nL Flow Cell ..............................95-96Diode Array Detector (DAD)/Multiple Wavelength Detector (MWD)...............93Evaporative Light Scattering Detector (ELSD) .....98Fluorescence Detector (FLD) .................................99Lamps ..........................................................................90Maintenance..............................................................89Maintenance Kits......................................................97Preparative Flow Cells.............................................96Refractive Index Detector (RID) ............................98Variable Wavelength Detector (VWD)...........91-92

Fittings and UnionsCapillary and Fittings Kits .................................36-39Fittings...................................................................40-41How to Align Connection Properly.......................45How to Prepare Connection...................................44How to Tighten Correctly........................................43

Fraction CollectorsCapillary Kits and Needles .....................................70Collecting Tubes and Trays.....................................69G1364D Micro Fraction Collector..........................71Maintenance Schedule ...........................................68Well Plate Trays ........................................................69

In-Line Filters ...............................................................12LC/MSChemicals.................................................................107Cleaning Supplies...................................................108Foreline Pump .........................................................107

Gas Purifiers ............................................................108Instrument Supplies.......................................105-106Maintenance Schedule .........................................103Preventive Maintenance Kit ................................104Quiet Cover ..............................................................109StandardsAnalyzer Kit............................................................110Calibrant Mixes.....................................................110Kits...........................................................................110

Tools...........................................................................108Loop Capillaries ...........................................................32Pumps1290 Infinity LC Pump Supplies ............................51Frits and Adapters ....................................................54Inlet Valves.................................................................49Kits..........................................................................59-60Outlet Valves..............................................................49Pistons and Seals .....................................................50Purge Valves ..............................................................48Routine Maintenance ..............................................47Safety Caps ................................................................55Seal Wash ..................................................................52Solvent Filters............................................................54Solvent Reservoir......................................................53Vacuum Degassers...................................................58

Rack for LC Systems..................................................14Solvent Filters/Degassers ........................................13Standards......................................................................15Thermostatted Column CompartmentCapillary Kits ........................................................83-88

Tools ...............................................................................11Troubleshooting.................................................546-549TubingAccessories................................................................35PEEK.............................................................................34Rigid Capillary Tubing ..............................................35

Unions............................................................................42ValvesInjection Valves.........................................................73Maintenance Notes .................................................72Manual Injection Valves with Position Sensing Switches .....................76-77Sample Loops ......................................................78-79Switching ValvesExternal Switching Valve......................................74Internal Switching Valve.......................................75

Syringes for Manual InjectionFitted Plungers........................................................80PTFE-Tipped Plungers............................................81

ApplicationsBioPharmaceutical ...................................................552Chemical/Industrial .................................................580Environmental............................................................583Food and Consumer Products ...............................594Pharmaceutical..........................................................611

CE and CE/MSAlignment Interface .................................................190CE/MS AccessoriesAdapter Kit ...............................................................194Capillaries .................................................................195Sprayer Kit................................................................195

CapillariesAlignment Interface ...............................................190Bulk Fused-Silica ....................................................181CEP Coated ..............................................................185Capillary Cassette...................................................190Capillary Electrochromatography (CEC)........188-189Cross-linked and Bonded µSIL....................186-187Extended Light Path (Bubble Cell) Bare Fused-Silica ..................179-180Polyvinyl Alcohol (PVA) Coated..................182-184Standard Bare Fused-Silica..................................178Universal Bare Fused-Silica .................................181

Capillary Cassette .....................................................190High Sensitivity Detection Cell......................191-192Instrument Supplies.................................................199Solution KitsCation ........................................................................173Forensics ..................................................................175Inorganic Anion...............................................171-172Organic Acids ..........................................................174µPAGE ...............................................................176-177

Standards & ReagentsCZE Buffers for Charged Analytes .....................196CZE Buffers for Proteins.......................................197Capillary Conditioning Solutions.........................196MEKC Buffers for Neutral and Charged Analytes...........................................197Plating Bath Analysis Buffer ...............................197Ultra Pure CE Water ..............................................196µPAGE Buffer Solutions and Oligo Standards...197

System Start-up and Test Kits ...............................198Troubleshooting.................................................201-203Vial Rack .....................................................................200Vials and Caps...........................................................199Window Etching Tool...............................................200

Columns for Biomolecule SeparationsAffinity ChromatographyAgilent Bio-Monolith Protein A ..................434-435Multiple Affinity Removal System..............438-440Multiple Affinity Removal System Starter Kits.....441Protein Fractionation System..............................437Proteomic Reagents ..............................................442mRP-C18 High-Recovery Protein ................442-443

Analysis ScaleCapillary and Nano.................................................452MicroBore (1.0 mm id) ..........................................461ZORBAX Bio-SCX Series II...................................458

CitationsPL-SAX......................................................................487PL-SCX ......................................................................487PLRP-S...............................................................486-487Poroshell 300...........................................................486ZORBAX 300............................................................485

Product Index

645

PRODUCT INDEX

WWW.AGILENT.COM/CHEM/LC

Column SelectionAmino Acid Analysis.............................................362Broad Distribution..................................................363DNA and RNA Oligonucleotide..........................360Natural and Synthetic Peptides .........................358Peptide Mapping....................................................356Protein ......................................................................353

Ion-Exchange ChromatographyAgilent Bio IEX .......................................................402Agilent Bio MAb ....................................................399Agilent Bio-Monolith ....................................412-413PL-SAX Strong Anion-Exchange........................406PL-SCX Strong Cation-Exchange .......................410

Literature............................................................477-484Method DevelopmentBio Ion-Exchange Column...................................447High Sensitivity Capillary Column......................451Reversed-Phase LC/MS Column.......................446SEC Column ....................................................449-450ZORBAX Columns..................................................444

Purification - Prep HPLCPL-SAX and PL-SCX......................................472-473PLRP-S..............................................................467-468Peptide PurificationVariPure IPE ..........................................................476VariTide RPC .........................................................475

ZORBAX PrepHT....................................................466Reversed-Phase HPLCPLRP-S .....................................................................387Poroshell 120 ..........................................................385Poroshell 300 ..................................................380-381ZORBAX 300Extend-C18 ......................................376ZORBAX 300StableBond......................................367ZORBAX Eclipse Amino Acid Analysis (AAA)........................394-395ZORBAX RRHD 300-Diphenyl .............................374

Size Exclusion Chromatography (SEC)Agilent Bio SEC-3 ..................................................418Agilent Bio SEC-5 ..................................................424ProSEC 300S ...........................................................428ZORBAX GF-250 and GF-450 ..............................431

Columns for Small MoleculeSeparationsColumn SelectionColumn and Mobile Phase Guidelines........211-213Method Development...................................220-221Quick Guide to Reversed-Phase.................207-209Small Molecule Overview............................218-219

Fast Columns for Reversed-Phase HPLC/UHPLCFast Guards for UHPLC ........................................246Poroshell 120 ..........................................................228ZORBAX Rapid Resolution High Definition (RRHD) 1.8 µm...........................233ZORBAX Rapid Resolution High Throughput (RRHT) 1.8 µm .......................239

Guard Columns.................................................223-224Kits for Analytical HPLCZORBAX Method Development Kits.........284-285ZORBAX Method Validation Kits ...............286-288

Oligo SolutionsStratoSpheres DNA Cartridges ..........................347TOP Cartridges ...............................................348-349

Other HPLC TechniquesHi-Plex for Carbohydrate Analysis.....................340ZORBAX HILIC Plus ..............................................324ZORBAX Ion-Exchange.........................................333ZORBAX Normal-Phase ...............................326-328

Preparative HPLCBulk Materials ........................................................321Load & Lock ............................................................322Polaris Prep .............................................................321Prep LC.............................................................311-312Pursuit and Pursuit XRs Prep .............................319ZORBAX PrepHT....................................................314

Reversed-Phase HPLCHC-C18(2).........................................................304-305PLRP-S .....................................................................306Polaris.......................................................................298Pursuit ..............................................................287-288TC-C18(2) .........................................................304-305ZORBAX 80Å Extend-C18 ....................................274ZORBAX 80Å StableBond....................................264ZORBAX Bonus-RP ...............................................278ZORBAX Eclipse PAH ...........................................254ZORBAX Eclipse Plus ...........................................248ZORBAX Eclipse XDB...........................................256ZORBAX Original....................................................283ZORBAX Rx .............................................................272

USP Designations ............................................343-346

CrossLab SuppliesAutosampler Maintenance....................................119Autosampler Syringes.....................................116-118CTC HPLC AutosamplersAutosampler Syringes ..........................................169

Capillaries and Tubing.............................................130Detector Lamps ........................................................113Dionex HPLC SystemsAutosampler Supplies...........................................158Autosampler Syringes ..........................................157Buffer Loops............................................................160Capillaries ........................................................166-168Detector Lamps......................................................157Fittings, Ferrules and Unions ..............................168In-Line Filters ..........................................................168Performance Maintenance Kits .................161-165Pump Maintenance Procedure...........................126Pump Supplies................................................158-159Sample Loops .........................................................160Tubing .......................................................................168Valve Replacement Parts.....................................159

Fittings ........................................................................131In-Line Filters ............................................................132Performance Maintenance Kits............................129Pump Maintenance .................................................124Pump Supplies..................................................122-123Sealing Mats .............................................................115Shimadzu HPLC SystemsAutosampler Syringes ..........................................150Capillaries ................................................................154Detector Lamps......................................................150Fittings, Ferrules and Unions ..............................155In-Line Filters ..........................................................156Performance Maintenance Kits .........................154

Pump Maintenance Procedure...........................125Pump Supplies................................................151-152Sample Loops .........................................................153Tubing .......................................................................155Valve Replacement Parts.............................152-153

Troubleshooting................................................133-136Valve Supplies...................................................127-128Waters HPLC SystemsAutosampler Syringes ..................................137-138Capillaries ................................................................148Detector Lamps......................................................137Detector Supplies ..................................................142Fittings, Ferrules and Unions ..............................149Performance Maintenance Kits .................144-158Pump Maintenance Procedure...........................124Pump Supplies................................................139-142Sample Loops .........................................................143Valve Replacement Parts.....................................142

Well Plates.................................................................115

GPC/SEC Columns and StandardsAqueousPL aquagel-OH Analytical....................................525PL aquagel-OH Preparative .................................528

Column Accessories................................................529OrganicPLgel Individual Pore Size ...................................505PLgel MIXED...................................................498-501PLgel MIXED-LS.....................................................502PLgel MiniMix.........................................................504PLgel Preparative...................................................506

Polymer StandardsEasiCal ......................................................................536EasiVial .....................................................................532Polyacrylic Acid......................................................545Polyethylene Glycol/Oxide..........................541-542Polymethylmethacrylate...............................539-540Polysaccharides .............................................543-544Polystyrene......................................................537-538

Setting Up a GPC/SEC System ....................491-495Special ApplicationEnviroPrep................................................................507MesoPore ................................................................520OligoPore .................................................................521PL HFIPgel ...............................................................509PL Rapide.........................................................510-511PLgel Olexis.............................................................508PlusPore...........................................................514-515PolarGel....................................................................512PolyPore ...................................................................516ResiPore...................................................................518

646

PART NUMBER INDEX

0100-0549 ..........................................1070100-0900.............................................420100-0969 ..........................................1050100-1259.............................................410100-1516................40, 92, 96, 99, 1060100-1543 ..........................................1950100-1597 ..........................................1070100-1631.............................................400100-1710......................................11, 580100-1847.............................................420100-1849......................................61, 730100-1850......................................75, 770100-1851 ........61, 73-75, 77, 101-1020100-1852.............................................750100-1853......................................61, 730100-1854....................................75, 1080100-1855...........................75, 104, 1080100-1859.............................................770100-1860.............................................770100-1921.............................................790100-1922.............................................790100-1923.............................................790100-1924.............................................790100-2051..................................104, 1080100-2086.............................................410100-2087.............................................750100-2088......................................61, 730100-2089.............................................750100-2175.............................................400100-2231......................................61, 730100-2233.............................................750100-2298.............................................420100-2304 ..........................................1060100-2410.............................................350100-2441.............................................420101-0376.............................................790101-0377.............................................790101-0378.............................................790101-0379.............................................790101-0620.............................................770101-0623.............................................770101-0921......................................61, 730101-1050......................................61, 730101-1219.............................................790101-1226.............................................790101-1227.............................................790101-1228.............................................790101-1229.............................................790101-1230.............................................790101-1231.............................................770101-1232.............................................770101-1233.............................................770101-1234.............................................790101-1235.............................................790101-1236.............................................790101-1237.............................................790101-1238.............................................790101-1239.............................................790101-1240.............................................790101-1241.............................................790101-1242.............................................790101-1243.............................................790101-1244.............................................790101-1245.............................................790101-1246.............................................790101-1247.............................................790101-1248.............................................790101-1249.............................................79

0101-1250.............................................790101-1251.............................................790101-1252.............................................790101-1253.............................................770101-1254.............................................770101-1255.............................................770101-1258.............................................750101-1267......................................61, 730101-1268......................................61, 730101-1288.......................................74-750101-1360.............................................750101-1362.............................................750101-1385......................................61, 730101-1409 .......................74-75, 77, 1020101-1415.......................................74-750101-1416.............................61, 73, 1010101-1417 ................................74-75, 770101-1421.......................................74-750101-1422......................................61, 730101-2415......................................61, 7301018-22707 ........................................4801018-23702 ........................................1101018-60025 ........................................5401018-68722 ........................................5901048-87302 ........................................2801078-87302..................................32, 6401078-87305 ........................................2801080-68702 ........................................1501080-68704 ........................................1501080-83202 ........................................4001090-27609 ........................................1201090-68702 ........................................1201090-68703 ........................................1201090-87304 ........................................2801090-87306..................................23, 3301090-87610 ........................................2301090-87611 ........................................2301100-68700 ........................................1105971-80103......................................10605980-60051......................................1080890-1727 ..........................................1070890-1761.............................................340890-1762.............................................340890-1763....................................34, 1020890-1915....................................34, 1060905-1163 ..........................................1990905-1175.............................................520905-1192.............................................480905-1294.............................................640905-1420.............................................510905-1516.............................................540905-1599.............................................640905-1717.............................................640905-1718.............................................520905-1719.............................................510905-1731 ..........................................10112102300............................................34912102301............................................349126-1012.............................................187126-1013.............................................187126-1713.............................................187127-1012.............................................187127-1712.............................................187127-1713.............................................1871400-0563 ..........................................10714251921............................................3491460-2571 .........................104-105, 1081520-0401 ..........................................195

1535-4045 ................................74-75, 771535-4046.............................................771535-4860.............................................791535-4970..................................104, 1071535-5045.............................................771535-5082.............................................77160-2644-5 .........................................181160-2650-5 .........................................181160-2660-5 .........................................181190-0131.............................................181190-0231.............................................181190-0331.............................................181190-0431.............................................181191-1311.............................................177191-3211.............................................177191-5211.............................................177192-1311.............................................176192-3211.............................................176192-5211.............................................176194-8111.............................................186196-7203.............................................186197-7202.............................................186199-2602.............................................186204310 ................................................4422140-0585 ..........................................1992140-0590.............................................902140-0600.............................................992140-0813.............................................902140-0820.............................................90280959-904 ..........................................12280959-907 ..........................................123150-0509.............................................133150-0576.............................................133150-0577.............................................133150-0619 ..........................................1993150-0944.............................................543162-0178 ..........................................1063162-1056 ..........................................1073162-1057 ..........................................107400510 ................................................442410910-101 ........................................313410910-102 ........................................313410910-301 ........................................313410910-302 ........................................313410910-501 ........................................313410910-502 ........................................313413910-101 ........................................313413910-102 ........................................313413910-301 ........................................313413910-302 ........................................313413910-501 ........................................313413910-502 ........................................313419910-301 ........................................313419910-302 ........................................313419910-501 ........................................313419910-502 ........................................313420212-901 ........................................313420212-902 ........................................313420420-901 ........................................313420910-901 ........................................313420910-902 ........................................313440905-901 ........................................313440905-902 ........................................313440910-901 ........................................313440910-902 ........................................313443905-101 ........................................313443905-102 ........................................313443905-901 ........................................313

443905-902 ........................................313443910-901 ........................................313443910-902 ........................................313446905-101 ........................................313446905-102 ........................................313446905-301 ........................................313446905-302 ........................................313446905-901 ........................................313446905-902 ........................................313446910-102 ........................................313449905-101 ........................................313449905-102 ........................................313449905-301 ........................................313449905-302 ........................................313449905-501 ........................................313449905-502 ........................................313449905-901 ........................................313449905-902 ........................................313449910-902 ........................................3135001-3702.............................................825001-3726.............................................145001-3743.............................................525021-1816.............................................285021-1817.............................................285021-1818.............................................285021-1819.......................................28-295021-1820.............................................275021-1821.............................................275021-1822.............................................275021-1823......................................27, 925021-1845..................................262, 2705021-1866.............................................115022-2133.............................................425022-2141 ..........................................1955022-2144.............................................425022-2145.............................................425022-2146.............................................955022-2155.............................................585022-2159.............................................275022-2165.............................................125022-2166.............................................125022-2175.............................................645022-2184......................................42, 955022-2185.............................................125022-2188.............................................515022-2192......................................48, 545022-6503.............................................825022-6509.............................................295022-6510.............................................295022-6531.............................................695022-6532.............................................695022-6533.............................................695022-6534.............................................695022-6536.............................................415022-6538......................................65, 695022-6539......................................65, 695022-6541.............................................715022-6542.............................................715022-6543.............................................715022-6544.............................................715022-6546.............................................715023-0208.............................................715023-0209.............................................715023-0213.............................................715023-0214.............................................715023-0215.............................................715023-0238.............................................715023-0271.............................................12

Part Number Index

647

PART NUMBER INDEX

5023-0282.............................................115023-1803.............................................425041-2168....................................54, 1995042-1385.............................................695042-1386.............................................695042-1388.............................................695042-1389.............................................695042-6454.............................................695042-6458.............................................695042-6459.............................................695042-6461.............................................345042-6462.............................................345042-6463.............................................345042-6470.............................................695042-6476.............................................155042-6478 ..........................................1995042-6491 ..........................................1995042-6500.............................................405042-8502.............................................695042-8507.............................................525042-8517......................................42, 715042-8518......................................42, 715042-8519......................................42, 715042-8922.............................................585042-8954.............................................525042-8957.............................................415042-9954.............................................115042-9967.............................................115043-0221.............................................565043-0222.............................................565043-0223.............................................565043-0224.............................................565043-0225.............................................565043-0226.............................................565043-0227.............................................565043-0228.............................................575043-0229.............................................575043-0230.............................................575043-0231.............................................575043-0232.......................................56-575043-0233.............................................575043-0234.............................................565043-0235.............................................575043-0236.............................................575043-0237.............................................575043-0238.............................................575043-0239.............................................575043-0242.............................................565043-0243.............................................565043-0255.............................................575043-0272.............................................565043-0300.............................................565043-0828.............................................565043-0829.............................................565043-0830.............................................565043-0831.............................................565043-0832.............................................565061-3303......................................40, 995061-3304.............................................395061-3315.............................................395061-3327.............................................995061-3328.............................................995061-3329.............................................995061-3330 ..........................................3955061-3331 ..........................................3955061-3332 ..........................................3955061-3333 ..........................................3955061-3334 ..........................................3955061-3335 ..........................................3955061-3337 ..........................................3955061-3339 ..........................................3955061-3361.............................................35

5061-3362.............................................355062-2418.............................................405062-2461.............................................235062-2462....................23-24, 33-34, 995062-2463......................................34, 995062-2478 ..........................................3955062-2479 ..........................................3955062-2483......................................34, 585062-2484.............................................525062-2486.............................................115062-8517....................................54, 1995062-8522......................................23, 925062-8524..................................172, 1755062-8529 ..........................................1925062-8534.............................................585062-8535 ...............................23, 33, 925062-8541.............................................405062-8544 ..........................................1995062-8562.............................................495062-8571 ..........................................1965062-8572 ..........................................1965062-8573 ..........................................1965062-8574 ..........................................1975062-8575..................................172, 1965062-8576.........................172, 174, 1965062-8577 ..........................................1965062-8578 .........................172-175, 1965062-8587.............................................645062-8588.............................................825063-6502.............................................775063-6506.............................................635063-6510 ..........................................1745063-6511 ..........................................1725063-6512 ..........................................1885063-6513 ..........................................1885063-6514 ..........................................1985063-6515 ..........................................1985063-6520 ..........................................1985063-6526.............................................825063-6531.............................................535063-6535 ..........................................1885063-6536 ..........................................1885063-6540 ..........................................1885063-6541 ..........................................1885063-6544 ..........................................1885063-6586......................................50, 645063-6589......................................51, 645063-6591.............................................405063-6592.............................................955063-6593......................................41, 955063-6597......................................15, 995063-6598.............................................585063-6599.............................................585064-8203 ..........................................1735064-8205 ..........................................1735064-8206 ..........................................1735064-8208 ..........................................1755064-8209 ..........................................1755064-8211.............................................115064-8220.............................................155064-8236 ..........................................1975064-8253 ..........................................2715064-8254 ..........................................2715064-8255 ..........................................2715064-8256 ..........................................2715064-8257 ..........................................2715064-8258..................................271, 4605064-8259..................................373, 4605064-8260 ..........................................2715064-8261 ..........................................2715064-8262 ..........................................2715064-8263..................................373, 460

5064-8264..................................373, 4605064-8265..................................373, 4605064-8266..................................373, 4605064-8267..................................373, 4605064-8268..................................373, 4605064-8269 ..........................................2635064-8270..................................373, 4605064-8271 ..........................................2635064-8273.............................................125064-8286 ..........................................2635064-8287 ..........................................2635064-8288 ..........................................2635064-8291 ..........................................2635064-8293.............................................645064-8294..................................373, 4605064-8295..................................373, 4605064-8296 ..........................................2635064-8297 ..........................................2635064-8298 ..........................................2635064-8300..................................373, 4605065-4402.............................................695065-4410.............................................415065-4420.............................................155065-4421.............................................535065-4422......................................41, 955065-4423.............................................415065-4426.............................................405065-4427 ..........................................4605065-4454.............................................405065-4459..................................373, 4605065-4460..................................373, 4605065-4461..................................373, 4605065-4462..................................373, 4605065-4463..................................373, 4605065-4464..................................379, 4605065-4465..................................379, 4605065-4466..................................379, 4605065-4467..................................379, 4605065-4468..................................384, 4605065-4498.............................................665065-4499.............................................605065-4500.............................................125065-9901.............................................125065-9908 ..........................................1105065-9910..................................373, 4605065-9911..................................373, 4605065-9912..................................458, 4605065-9913..................................373, 4605065-9914..................................373, 4605065-9915..................................373, 4605065-9922.............................................605065-9923..................................373, 4605065-9924..................................373, 4605065-9926.............................................295065-9927.............................................295065-9931.............................................285065-9932.............................................285065-9933.......................................28-295065-9935.............................................275065-9937.............................................365065-9938.............................................365065-9939.............................................375065-9942..................................458, 4605065-9947......................................37, 825065-9948......................................35, 415065-9950......................................35, 415065-9952.............................................525065-9963.............................................285065-9964.............................................275065-9967.............................................405065-9971......................................34, 425065-9976.............................................34

5065-9978......................................34, 525067-1540.............................................415067-1547.............................................415067-1551.............................................125067-1553.............................................125067-1555.............................................125067-1557.............................................415067-1558.............................................415067-1562.............................................125067-1565.............................................545067-1581.............................................775067-1582 ..........................................1005067-1584 ..........................................1005067-1585 ..........................................1005067-1595.............................................845067-1596.............................................855067-1597.............................................855067-4104.............................................775067-4105.............................................775067-4107.............................................755067-4108.............................................755067-4111.............................................755067-4112.............................................755067-4113.............................................755067-4114......................................61, 735067-4117.......................................74-755067-4118.......................................74-755067-4121.............................................755067-4124.............................................515067-4131....................................74, 1015067-4132.......................................74-755067-4134.......................................74-755067-4137.............................................755067-4141.............................................775067-4142.......................................74-755067-4144.......................................74-755067-4146.......................................74-755067-4148.......................................74-755067-4158.............................................775067-4159..............................74-75, 1025067-4170.............................................755067-4174.............................................485067-4202.............................................775067-4601.......................................83-855067-4607.............................................295067-4608.......................................28-295067-4609.............................................295067-4633.............................................375067-4638.............................................125067-4646 ...............................38, 84, 865067-4647.............................................255067-4648.............................................285067-4649.............................................255067-4650.............................................255067-4651.............................................255067-4653.............................................265067-4657.............................................245067-4658.............................................245067-4659.............................................245067-4660.............................................245067-4661.............................................515067-4662.............................................675067-4669.............................................245067-4670.............................................245067-4678.............................................505067-4682......................................38, 865067-4684.............................................255067-4685.............................................285067-4686.............................................255067-4687.............................................255067-4688.............................................285067-4689.............................................26


648

PART NUMBER INDEX

5067-4695.....................50, 64, 101-1025067-4697.............................................515067-4699.............................................595067-4703......................................32, 645067-4710......................................32, 645067-4716.............................................515067-4717.............................................515067-4728.......................................48-495067-4729......................................39, 875067-4730.............................................875067-4733.............................................405067-4735.............................................255067-4737.............................................285067-4738.............................................405067-4739.............................................405067-4741....................................42, 1025067-4744.............................................255067-4745.............................................255067-4746.............................................265067-4767.............................................885067-4769.............................................885067-4777.............................................295067-4778.............................................295067-4779.............................................295067-4780.............................................295067-4781.............................................295067-4782.............................................295067-4798.............................................585067-4800.............................................875067-5103......................................38, 885067-5104.............................................255067-5106.............................................255067-5107.............................................255067-5109.............................................265067-5110.............................................265067-5111.............................................265067-5112.............................................265067-5113.............................................265067-5120.............................................285067-5189.............................................395067-5378.............................................585067-5380.............................................585067-5383.............................................585068-0001.............................................755068-0002.............................................755068-0004.............................................485068-0005.............................................485068-0006.......................................74-755068-0007......................................61, 735068-0008.......................................74-755068-0011.......................................74-755068-0012.......................................74-755068-0040..............................74-75, 1025068-0041..............................74-75, 1025068-0044.......................................74-755068-0045..............................74-75, 1025068-0052.............................................775068-0053.............................................775068-0060 ...............74-75, 77, 101-1025068-0067.......................................74-755068-0076.......................................74-755068-0077.......................................74-755068-0082.............................................775068-0093.......................................74-755068-0095.......................................74-755068-0097.......................................74-755068-0115.............................................755068-0116.............................................755068-0122.............................................485068-0123.............................................485069-3635 ..........................................4125069-3636 ..........................................412

5069-3637 ..........................................4125069-3639 ..........................................4355080-5400 ..........................................1085133001..............................................3495133005..............................................3495180-4108......................................40, 995180-4114......................................40, 995181-1507 ..........................................1995181-1512 ..........................................1995181-1513 ..........................................1995181-1541.............................................715181-8836 ..........................................2005182-0567 ..........................................1995182-1530.............................................905182-9697 ..........................................1995182-9710 ..........................................1065183-2021 ..........................................2855183-2022 ..........................................2855183-4619 ..........................................1995183-4623 ..........................................1995183-4624 ..........................................2855183-4625 ..........................................2855183-4626 ..........................................2855183-4627 ..........................................2855183-4669 ..........................................2005183-4670 ..........................................2005185-5807 ..........................................2855185-5808 ..........................................2855185-5809 ..........................................2855185-5810 ..........................................2855185-5920.........................269, 372, 4635185-5921 ..........................................2615185-5922 ..........................................2825185-5923 ..........................................2775185-5968..................................384, 4635185-5984 ..........................................4395185-5985 ..........................................4395185-5986 ..........................................4415185-5987 ..........................................4415185-5988 ..........................................4415185-5990 ..........................................4415185-5991 ..........................................4415188-2743.............................................135188-2744.............................................135188-2745.............................................135188-2746.............................................135188-5217 ..........................................4395188-5218 ..........................................4395188-5230 ..........................................4395188-5231 ..........................................4425188-5249 ..........................................4415188-5250 ..........................................4415188-5251 ..........................................4415188-5252 ..........................................4415188-5253 ..........................................4415188-5254 ..........................................4415188-5289 ..........................................4395188-5321.............................................695188-5322.............................................695188-5332 ..........................................4395188-5333 ..........................................4395188-5334 ..........................................4395188-5336 ..........................................4395188-5341 ..........................................4395188-6408 ..........................................4395188-6409 ..........................................4395188-6410 ..........................................4395188-6411 ..........................................4395188-6510 ..........................................4425188-6511 ..........................................4425188-6523 ..........................................1105188-6529.............................................15

5188-6557 ..........................................4395188-6558 ..........................................4395188-6559 ..........................................4395188-6560 ..........................................4395188-6562 ..........................................4395188-8283 ..........................................4415188-8825 ..........................................4395188-8826 ..........................................4395190-0443 ..........................................1105190-0469 ..........................................1105190-0488.............................................155190-0551 ..........................................1105190-0554 ..........................................1105190-0555 ..........................................1105190-0556 ..........................................1105190-0917....................................90, 1995190-0924.............................................115190-1401 ..........................................1085190-1431 ..........................................2845190-1432 ..........................................2845190-1433 ..........................................2845190-1434 ..........................................2845190-1435 ..........................................2845190-1436 ..........................................2845190-1443 ..........................................1045190-1480.............................................805190-1484.............................................805190-1485.............................................805190-1486.......................................80-815190-1492.............................................815190-1494.............................................805190-1499.............................................815190-1501.............................................805190-1505.............................................815190-1508.............................................805190-1512.............................................815190-1515.............................................805190-1520.............................................815190-1522.............................................805190-1526.............................................815190-1558.............................................815190-1560.............................................815190-1561.............................................815190-1562.............................................815190-1564.............................................815190-1571.............................................815190-2401 ..........................................4015190-2402 ..........................................4015190-2403 ..........................................4015190-2404 ..........................................4015190-2405 ..........................................4015190-2406 ..........................................4015190-2407 ..........................................4015190-2408 ..........................................4015190-2411 ..........................................4015190-2412 ..........................................4015190-2413 ..........................................4015190-2414 ..........................................4015190-2415 ..........................................4015190-2416 ..........................................4015190-2419 ..........................................4015190-2420 ..........................................4015190-2421 ..........................................4055190-2422 ..........................................4055190-2423 ..........................................4055190-2424 ..........................................4055190-2425 ..........................................4055190-2426 ..........................................4055190-2427 ..........................................4055190-2428 ..........................................4055190-2431 ..........................................4055190-2432 ..........................................405

5190-2433 ..........................................4055190-2434 ..........................................4055190-2435 ..........................................4055190-2436 ..........................................4055190-2439 ..........................................4055190-2440 ..........................................4055190-2441 ..........................................4055190-2442 ..........................................4055190-2443 ..........................................4055190-2444 ..........................................4055190-2445 ..........................................4055190-2446 ..........................................4055190-2447 ..........................................4055190-2448 ..........................................4055190-2451 ..........................................4055190-2452 ..........................................4055190-2453 ..........................................4055190-2454 ..........................................4055190-2455 ..........................................4055190-2456 ..........................................4055190-2459 ..........................................4055190-2460 ..........................................4055190-2461 ..........................................4055190-2462 ..........................................4055190-2463 ..........................................4055190-2464 ..........................................4055190-2465 ..........................................4055190-2466 ..........................................4055190-2467 ..........................................4055190-2468 ..........................................4055190-2471 ..........................................4055190-2472 ..........................................4055190-2473 ..........................................4055190-2474 ..........................................4055190-2475 ..........................................4055190-2476 ..........................................4055190-2479 ..........................................4055190-2480 ..........................................4055190-2481 ..........................................4055190-2482 ..........................................4055190-2483 ..........................................4055190-2484 ..........................................4055190-2485 ..........................................4055190-2486 ..........................................4055190-2487 ..........................................4055190-2488 ..........................................4055190-2491 ..........................................4055190-2492 ..........................................4055190-2493 ..........................................4055190-2494 ..........................................4055190-2495 ..........................................4055190-2496 ..........................................4055190-2499 ..........................................4055190-2500 ..........................................4055190-2501 ..........................................4235190-2502 ..........................................4235190-2503 ..........................................4235190-2504 ..........................................4235190-2505 ..........................................4235190-2506 ..........................................4235190-2507 ..........................................4235190-2508 ..........................................4235190-2509 ..........................................4235190-2510 ..........................................4235190-2511 ..........................................4235190-2512 ..........................................4235190-2513 ..........................................4235190-2514 ..........................................4235190-2515 ..........................................4235190-2516 ..........................................4275190-2517 ..........................................4275190-2518 ..........................................427

649

PART NUMBER INDEX

5190-2519 ..........................................4275190-2520 ..........................................4275190-2521 ..........................................4275190-2522 ..........................................4275190-2523 ..........................................4275190-2524 ..........................................4275190-2525 ..........................................4275190-2526 ..........................................4275190-2527 ..........................................4275190-2528 ..........................................4275190-2529 ..........................................4275190-2530 ..........................................4275190-2531 ..........................................4275190-2532 ..........................................4275190-2533 ..........................................4275190-2534 ..........................................4275190-2535 ..........................................4275190-2536 ..........................................4275190-2537 ..........................................4275190-2538 ..........................................4275190-2539 ..........................................4275190-2540 ..........................................4275190-2541 ..........................................4275190-2542 ..........................................4275190-2543 ..........................................4275190-2544 ..........................................4275190-2545 ..........................................427520518-904 ........................................305520518-905 ........................................305588905-902 ........................................305588915-902 ........................................305588925-902 ........................................305588935-902 ........................................305590-3003.............................................200590-4000....................................177, 197590-4001....................................177, 197590-4005....................................177, 19759980-20134......................................10759987-20033......................................10759987-20040......................................1056040-0798 ..........................................1076040-0834..................................104, 107660750-902 ...............................210, 384660750-906 ........................................384660750-909 ........................................384661750-902 ...............................384, 463661750-906 ...............................384, 463661750-909 ...............................384, 463670750-902 ........................................384671750-902 ...............................384, 463681775-902 ........................................229681975-302 ........................................229681975-902 ........................................229683775-902 ...............................229, 386683775-906 ........................................229683775-914 ........................................229683975-302 ...............................229, 386683975-306 ........................................229683975-314 ........................................229683975-902 ...............................229, 386683975-906 ........................................229683975-914 ........................................229685775-902 ...............................229, 386685775-906 ........................................229685775-914 ........................................229685975-302 ...............................229, 386685975-306 ........................................229685975-314 ........................................229685975-902 ...............................229, 386685975-906 ........................................229685975-914 ........................................229687775-902 ........................................229

687975-302 ........................................229687975-902 ........................................229689775-902 ........................................229689775-906 ........................................229689775-914 ........................................229689975-302 ........................................229689975-306 ........................................229689975-314 ........................................229689975-902 ........................................229689975-906 ........................................229689975-914 ........................................229691775-902 ........................................229691775-906 ........................................229691975-302 ........................................229691975-306 ........................................229691975-902 ........................................229691975-906 ........................................229693768-901 ........................................229693775-901 ........................................325693775-902 ...............................229, 386693775-906 ........................................229693775-912 ........................................229693968-301 ........................................229693968-901 ........................................229693975-301 ........................................325693975-302 ...............................229, 386693975-306 ........................................229693975-312 ........................................229693975-901 ........................................325693975-902 ...............................229, 386693975-906 ........................................229693975-912 ........................................229695768-901 ........................................229695775-901 ........................................325695775-902 ...............................229, 386695775-906 ........................................229695775-912 ........................................229695968-301 ........................................229695968-901 ........................................229695975-302 ...............................229, 386695975-306 ........................................229695975-312 ........................................229695975-901 ........................................325695975-902 ......................210, 229, 386695975-906 ........................................229695975-912 ........................................229697775-902 ........................................229697775-906 ........................................229697975-302 ........................................229697975-306 ........................................229697975-902 ...............................210, 229697975-906 ........................................229699768-901 ........................................229699775-901 ........................................325699775-902 ........................................229699775-906 ........................................229699775-912 ........................................229699968-301 ........................................229699968-901 ........................................229699975-301 ........................................325699975-302 ........................................229699975-306 ........................................229699975-312 ........................................229699975-901 ........................................325699975-902 ........................................229699975-906 ........................................229699975-912 ........................................229722975-902 ........................................245724700-902 ...............................243, 277724975-302 ...............................243, 277724975-902 ...............................243, 276726700-902 ...............................243, 277

726975-302 ...............................243, 277726975-902 ...............................243, 276727700-902 ...............................243, 277727975-302 ...............................243, 277727975-902 ...............................243, 276728700-902 ...............................243, 277728975-302 ...............................243, 277728975-902 ...............................243, 276735700-902 ........................................277735953-902 ........................................276735954-302 ........................................276746450-902 ........................................27675400001............................................34975700001............................................3497571901C ...........................................34975719025............................................34975719050............................................3497572915B ...........................................3497572915C ...........................................3497573915B ...........................................3497573915C ...........................................349757700-302 ...............................238, 277757700-902 ...............................238, 277758700-302 ...............................238, 277758700-902 ...............................238, 277759700-302 ........................................238759700-902 ...............................238, 277760450-902 ........................................277761600-902 ........................................277761753-902 ........................................277761775-902 ........................................379761973-902 ........................................379763600-902 ........................................277763750-902 ........................................379763953-902 ........................................276763954-302 ........................................276763973-902 ........................................379764953-302 ........................................276764953-902 ........................................276765600-902 ........................................277765750-902 ........................................379765973-902 ........................................379766953-902 ........................................276770050-902 ...............................277, 318770100-902 ...............................277, 318770150-902 ...............................277, 318770450-302 ........................................276770450-902 ........................................276770995-902 ........................................379773450-302 ........................................276773450-902 ........................................276773700-902 ........................................277773995-902 ........................................37979835-87638 ........................................2979841-87610 ........................................277995108-344......................................2627995108-585......................................2627995108-595......................................2627995118-344......................................2627995118-504 .............................262, 2707995118-585......................................2627995118-595......................................2627995208-344......................................2707995208-585......................................2707995208-595......................................2707995218-344......................................2707995218-585..............................270-2717995218-595......................................2707995230-344......................................2628001-0401 ..........................................1508001-0402 ..........................................1508001-0403 ..........................................150

8001-0405 ..........................................1508001-0406 ..........................................1508001-0501 ..........................................1518001-0502 ..........................................1518001-0503 ..........................................1518001-0504 ..........................................1518001-0506 ..........................................1528001-0509 ..........................................1548001-0510 ..........................................1528001-0511 ..........................................1528001-0512 ..........................................1528001-0513 ..........................................1528001-0514 ..........................................1518001-0515 ..........................................1518001-0516 ..........................................1528001-0517 ..........................................1548001-0519 ..........................................1528001-0520 ..........................................1528001-0521 ..........................................1528001-0522 ..........................................1518001-0527 ..........................................1528001-0528 ..........................................1528001-0529 ..........................................1528001-0530 ..........................................1528001-0531 ..........................................1528001-0532 ..........................................1528001-0533 ..........................................1518001-0534 ..........................................1518001-0535 ..........................................1528001-0601 ..........................................1538001-0603 ..........................................1538001-0604 ..........................................1538001-0607 ..........................................1538001-0608 ..........................................1538001-0609 ..........................................1538001-0610 ..........................................1548001-0612 ..........................................1538001-0613 ..........................................1538001-0614 ..........................................1538001-0615 ..........................................1528001-0701 ..........................................1508001-0702 ..........................................1508001-0703 ..........................................1508001-0704 ..........................................1508001-0705 ..........................................1508001-0801 ..........................................1538001-0802 ..........................................1538001-0803 ..........................................1558001-0805 ..........................................1558001-0806 ..........................................1558001-0807 ..........................................1558001-0808 ..........................................1568001-0809 ..........................................1538001-0810 ..........................................1548001-0812 ..........................................1538001-0813 ..........................................1558001-0814 ..........................................1538001-0816 ..........................................1558001-0817 ..........................................1558001-0818 ..........................................1548001-0819 ..........................................1558001-0821 ..........................................1548001-0822 ..........................................1548001-0823 ..........................................1558001-0824 ..........................................1558001-8020 ..........................................1548002-0401 ..........................................1578002-0402 ..........................................1578002-0403 ..........................................1578002-0404 ..........................................1578002-0405 ..........................................1578002-0406 ..........................................157


650

PART NUMBER INDEX

8002-0407 ..........................................1578002-0408 ..........................................1578002-0412 ..........................................1578002-0413 ..........................................1578002-0414 ..........................................1578002-0415 ..........................................1578002-0501 ..........................................1588002-0502 ..........................................1588002-0515 ..........................................1588002-0516 ..........................................1598002-0517 ..........................................1598002-0601 ..........................................1588002-0602 ..........................................1598002-0603 ..........................................1598002-0604 ..........................................1598002-0605 ..........................................1598002-0607 ..........................................1598002-0608 ..........................................1598002-0610 ..........................................1658002-0611 ..........................................1658002-0701 ..........................................1578002-0702 ..........................................1578002-0703 ..........................................1578002-0704 ..........................................1578002-0705 ..........................................1578002-0706 ..........................................1578002-0802 ..........................................1688002-0803 ..........................................1688002-0805 ..........................................1688002-0806 ..........................................1688002-0808 ..........................................1588002-0809 ..........................................1588002-0810 ..........................................1588002-0811 ..........................................1608002-0815 ..........................................1678002-0816 ..........................................1678002-0817 ..........................................1678002-0818 ..........................................1668002-0819 ..........................................1668002-0820 ..........................................1668002-0821 ..........................................1668002-0822 ..........................................1668002-0823 ..........................................1668002-0824 ..........................................1668002-0825 ..........................................1668002-0826 ..........................................1668002-0831 ..........................................1668002-0832 ..........................................1668002-0833 ..........................................1668002-0834 ..........................................1668002-0835 ..........................................1678002-0837 ..........................................1668002-0856 ..........................................1608002-0857 ..........................................1608002-0858 ..........................................1608002-0859 ..........................................1608002-0860 ..........................................1608002-0901 ..........................................1648002-0902 ..........................................1648002-0903 ..........................................1648002-0904 ..........................................1638002-0905 ..........................................1648002-0906 ..........................................1638002-0907 ..........................................1618002-0908 ..........................................1618002-0909 ..........................................1628002-0910 ..........................................1628002-0911 ..........................................1618002-0912 ..........................................1628002-0913 ..........................................1638002-0915 ..........................................1658002-0916 ..........................................165

8002-0917 ..........................................1618002-0918 ..........................................1628002-0919 ..........................................1628002-0921 ..........................................1688002-0923 ..........................................1648002-0924 ..........................................1648005-0414 ..........................................1388005-0416 ..........................................1388005-0417 ..........................................1388005-0418 ..........................................1388005-0419 ..........................................1388005-0420 ..........................................1388005-0422 ..........................................1388005-0423 ..........................................1388005-0508 ..........................................1418005-0512 ..........................................1428005-0513 ..........................................1418005-0514 ..........................................1398005-0515 ..........................................1408005-0516 ..........................................1408005-0523 ..........................................1408005-0524 ..........................................1418005-0525 ..........................................1418005-0526 ..........................................1418005-0527 ..........................................1408005-0528..................................142, 1458005-0529 ..........................................1408005-0530 ..........................................1408005-0531 ..........................................1408005-0532 ..........................................1428005-0533 ..........................................1408005-0535 ..........................................1398005-0536 ..........................................1398005-0537 ..........................................1418005-0538 ..........................................1398005-0539 ..........................................1408005-0540 ..........................................1408005-0541 ..........................................1398005-0601 ..........................................1428005-0602 ..........................................1428005-0603 ..........................................1428005-0604 ..........................................1428005-0605 ..........................................1428005-0702 ..........................................1378005-0704 ..........................................1378005-0705 ..........................................1378005-0812 ..........................................1488005-0822 ..........................................1488005-0823 ..........................................1488005-0824 ..........................................1488005-0825 ..........................................1488005-0826 ..........................................1488005-0835 ..................................148-1498005-0836 ..........................................1498005-0837 ..........................................1498005-0838.........................143, 149, 1568005-0839 ..........................................1438005-0840 ..........................................1438005-0841 ..........................................1438005-0842 ..........................................1438005-0843 ..........................................1438005-0844 ..........................................1438005-0845 ..........................................1438005-0846 ..........................................1438005-0901 ..........................................1468005-0902 ..........................................1468005-0903 ..........................................1468005-0904 ..........................................1468005-0905 ..........................................1478005-0906 ..........................................1478005-0907 ..........................................1468005-0908 ..........................................147

8005-0911 ..........................................1458005-0912 ..........................................1458005-0913 ..........................................1448005-0914 ..........................................1468005-0915 ..........................................1448005-0916 ..........................................1448005-0925 ..........................................1458005-0926 ..........................................1458005-0927 ..........................................1468005-0928 ..........................................1448005-0929 ..........................................1458005-0930 ..........................................1448010-0440 ..........................................1698010-0441..................................137, 1698010-0442..................................137, 1698010-0443..................................137, 1698010-0444..................................137, 1698010-0445..................................137, 1698010-0446..................................137, 1698010-0448..................................137, 1698010-0449 ..........................................1698010-0450..................................137, 1698010-0455..................................137, 1698010-0456..................................137, 1698010-0457..................................137, 1698010-0458..................................137, 1698010-0459..................................137, 1698010-0460..................................137, 1698010-0467..................................137, 1698010-0468..................................137, 169820212-911 ........................................433820212-914 ...............................273, 318820212-915 ......................269, 273, 317820212-918 ......................317, 373, 466820212-919 ...............................318, 329820212-920 ...............................269, 317820212-921 ......................317, 373, 466820212-924 ......................317, 373, 466820212-925 ...............................261, 318820212-926 ...............................261, 318820212-928 ...............................282, 318820212-930 ...............................277, 318820212-933 ...............................269, 317820385-901 ........................................318820400-901 ............261, 269, 273, 277,

282-283, 313, 317-318, 329-330, 373, 433, 466

820444-901 ............261, 269, 273, 277, 282, 313, 317-318,

329-330, 373, 433, 466820555-901 ......................245, 263, 270820675-111 ...............................330, 433820675-112 ........................................261820675-115 ......................269, 273, 283820675-119 ................................329-330820675-124 ......................269, 283, 372820700-902 ...............................244, 269820700-905 ...............................244, 269820700-906 ...............................244, 269820700-912 ...............................244, 269820750-901 ......................243, 246, 252820750-902 ......................244, 246, 267820750-903 ......................243, 246, 260820750-904 ......................244, 246, 267820750-911 ...............................229, 246820750-912 ...............................229, 246820750-913 ...............................229, 246820750-914 ...............................229, 246820950-901 ........................................330820950-902 ........................................283820950-905 ...............................283, 330820950-906 ........................................283

820950-908 ........................................330820950-911 ........................................433820950-912 ........................................283820950-913 ........................................273820950-914 ........................................273820950-915 ........................................269820950-916 ........................................269820950-917 ........................................269820950-918 ........................................372820950-919 ........................................329820950-920 ........................................269820950-921 ........................................372820950-922 ........................................269820950-923 ........................................372820950-924 ...............................283, 372820950-925 ........................................261820950-926 ........................................261820950-927 ........................................261820950-928 ........................................282820950-930 ........................................277820950-931 ........................................394820950-932 ........................................379820950-933 ........................................269820950-935 ...............................261, 329820950-936 ........................................253820950-937 ........................................253820950-938 ........................................253820950-939 ...............................253, 255820999-901 ............225, 253, 255, 261,

269, 273, 277, 282-283, 305, 329-330, 334, 372,

379, 384, 394, 433821075-918 ........................................384821075-920 ........................................384821075-924 ........................................384821125-915 ...............................269, 273821125-918 ........................................372821125-919 ........................................329821125-924 ...............................269, 372821125-926 ........................................261821125-928 ........................................282821125-930 ........................................277821125-932 ........................................379821125-933 ........................................269821125-935 ...............................261, 329821125-936 ........................................253821125-937 ........................................253821125-938 ........................................253821125-939 ...............................253, 255821700-902 ...............................245, 270821700-932 ...............................245, 270821725-901 .............238, 243, 246, 253821725-902 .............238, 244, 246, 269821725-903 .............238, 243, 246, 261821725-904 .............238, 244, 246, 269821725-911 ...............................229, 246821725-912 ...............................229, 246821725-913 ...............................229, 246821725-914 ...............................229, 246821975-902 ...............................245, 270821975-932 ...............................245, 270822700-902 ........................................270822700-932 ........................................270822975-902 .......................244-245, 270822975-906 ...............................245, 270822975-932 ........................................270823700-902 ...............................245, 270823700-932 ...............................245, 270823750-901 .............238, 243, 246, 253823750-902 .............238, 244, 246, 268823750-903 .............238, 243, 246, 260823750-904 .............238, 244, 246, 268

651

PART NUMBER INDEX

823750-911 ...............................229, 246823750-912 ...............................229, 246823750-913 ...............................229, 246823750-914 ...............................229, 246823975-902 ...............................245, 270823975-932 ...............................245, 270824700-902 ...............................244, 269824700-905 ...............................244, 269824700-906 ...............................244, 269824700-912 ...............................244, 269824700-914 ...............................244, 269824975-302 ...............................244, 268824975-305 ...............................244, 268824975-306 ...............................244, 268824975-902 ...............................244, 267824975-905 ...............................244, 267824975-906 ...............................244, 267824975-912 ...............................244, 267824975-914 ...............................244, 267825700-902 ...............................245, 270825700-932 ...............................245, 270825975-902 ...............................245, 270825975-932 ...............................245, 270826700-902 ...............................244, 269826700-906 ...............................244, 269826975-302 ...............................244, 268826975-306 ...............................244, 268826975-902 ...............................244, 267826975-906 ...............................244, 267827668-301 ...............................244, 281827668-901 ...............................244, 281827700-901 ...............................244, 329827700-902 ...............................244, 269827700-905 ...............................244, 269827700-906 ...............................244, 269827700-912 ...............................244, 269827700-914 ...............................244, 269827768-901 ...............................244, 282827975-301 ...............................244, 329827975-302 ...............................244, 268827975-305 ...............................244, 268827975-306 ...............................244, 268827975-312 ...............................244, 268827975-314 ...............................244, 268827975-901 ........................................244827975-902 ......................244, 267, 329827975-905 ...............................244, 267827975-906 ...............................244, 267827975-912 ...............................244, 267827975-914 ...............................244, 267828668-301 ...............................244, 281828668-901 ...............................244, 281828700-901 ...............................244, 329828700-902 ...............................244, 269828700-905 ...............................244, 269828700-906 ...............................244, 269828700-912 ...............................244, 269828700-914 ...............................244, 269828768-901 ...............................244, 282828975-301 ...............................244, 329828975-302 ...............................244, 268828975-305 ...............................244, 268828975-306 ...............................244, 268828975-309 ........................................268828975-312 ...............................244, 268828975-314 ...............................244, 268828975-901 ...............................244, 329828975-902 ...............................244, 267828975-905 ...............................244, 267828975-906 ...............................244, 267828975-912 ...............................244, 267828975-914 ...............................244, 267

829975-302 ...............................244, 268829975-305 ...............................244, 268829975-306 ...............................244, 268829975-312 ...............................244, 268829975-902 ...............................244, 267829975-905 ...............................244, 267829975-906 ...............................244, 267829975-912 ...............................244, 267829975-914 ...............................244, 267830668-901 ...............................244, 281830975-906 ...............................244, 267830990-902 ........................................268830990-906 ........................................268830990-914 ........................................268831975-902 ........................................270831975-906 ........................................270831975-932 ........................................270831975-936 ........................................270832975-902 ........................................267832975-906 ........................................267833975-902 ........................................270833975-906 ........................................270833975-912 ........................................270833975-932 ........................................270833975-936 ........................................270834975-902 ........................................267834975-906 ........................................267835668-901 ........................................281835975-902 ........................................267835975-905 ........................................267835975-906 ........................................267835975-912 ........................................267835975-914 ........................................267840140-901 ............261, 269, 273, 283,

329-330, 372, 433840300-908 ........................................330843300-908 ........................................330846952-704 ........................................334846975-202 ........................................267846975-902 ........................................267846975-906 ........................................267846975-914 ........................................2678500-1867 ..........................................1078500-2236 ..........................................1078500-4410 ..........................................1958500-6762.............................................158500-6782 ..........................................1968500-6785 ..........................................1748500-6786 ..........................................1978500-6787 ..........................................1978500-6797 ..........................................1728500-6900 ..........................................1748500-6917 ..........................................110857700-302 ...............................238, 268857700-305 ...............................238, 268857700-306 ...............................238, 268857700-312 ...............................238, 268857700-314 ........................................238857700-902 ...............................238, 268857700-905 ...............................238, 268857700-906 ...............................238, 268857700-912 ...............................238, 268857700-914 ........................................238857750-902 ........................................372857750-906 ........................................372857750-909 ........................................372857750-944 ...............................372, 375857768-901 ...............................238, 281858700-302 ...............................238, 268858700-305 ...............................238, 268858700-306 ...............................238, 268858700-312 ........................................268

858700-314 ........................................238858700-902 ...............................238, 268858700-905 ...............................238, 268858700-906 ...............................238, 268858700-912 ...............................238, 268858700-914 ........................................238858750-902 ........................................372858750-906 ........................................372858750-909 ........................................372858750-944 .......................372, 374-375858768-901 ...............................238, 281859700-302 ...............................238, 268859700-306 ...............................238, 268859700-902 ...............................238, 268859700-905 ...............................238, 268859700-906 ...............................238, 268859700-912 ...............................238, 268859700-914 ........................................238859768-901 ...............................238, 281860700-304 ........................................334860700-704 ........................................334860700-708 ........................................330860950-902 ........................................372860950-905 ........................................372860950-906 ........................................372860950-909 ........................................372860975-902 ........................................268860975-905 ........................................268860975-906 ........................................268860975-909 ........................................268860975-912 ........................................268860975-914 ........................................268861600-902 ........................................269861600-906 ........................................269861608-901 ........................................282861630-902 ...............................372, 463861700-901 ........................................282861753-902 ........................................268861753-905 ........................................268861753-906 ........................................268861753-912 ........................................268861753-914 ........................................268861767-902 ........................................273861768-901 ........................................282861775-902 ........................................372861775-906 ........................................372861953-902 ........................................267861953-905 ........................................267861953-906 ........................................267861953-912 ........................................267861953-914 ........................................267861954-302 ........................................267861954-305 ........................................267861954-306 ........................................267861954-309 ........................................267861954-312 ........................................267861954-314 ........................................267861967-302 ........................................273861967-902 ........................................273861971-901 ........................................281861973-306 ........................................372861973-902 ........................................372861973-906 ........................................372863600-902 ........................................269863600-905 ........................................269863600-906 ........................................269863608-901 ........................................282863630-902 ...............................372, 463863630-906 ...............................372, 463863668-301 ........................................281863668-901 ........................................281863700-901 ........................................282

863750-906 ........................................372863953-902 ........................................267863953-905 ........................................267863953-906 ........................................267863953-912 ........................................267863953-914 ........................................267863954-302 ........................................267863954-305 ........................................267863954-306 ........................................267863954-312 ........................................267863954-314 ........................................267863967-302 ........................................273863967-902 ........................................273863973-902 ...............................210, 372863973-905 ........................................372863973-906 ........................................372863973-909 ........................................372863974-302 ........................................372863974-306 ........................................372863974-309 ........................................372864668-301 ........................................281864668-901 ........................................281865600-902 ........................................269865600-906 ........................................269865608-901 ........................................282865630-902 ...............................372, 463865630-906 ...............................372, 463865750-902 ........................................372865750-906 ........................................372865973-902 ...............................210, 372865973-905 ........................................372865973-906 ........................................372865973-909 ........................................3728660-0827 ..........................................108866668-901 ........................................281866735-902 ........................................268866953-302 ........................................267866953-902 ........................................267866953-905 ........................................267866953-906 ........................................267866953-912 ........................................267866953-914 ........................................267866967-902 ........................................273868050-901 ...............................282, 318868100-901 ...............................282, 318868150-901 ...............................282, 318870050-902 ...............................269, 317870050-906 ...............................269, 317870050-914 ...............................269, 317870100-902 ...............................269, 317870100-906 ...............................269, 317870100-914 ...............................269, 317870150-902 ...............................269, 317870150-906 ...............................269, 317870150-914 ...............................269, 3178710-0004 ..........................................1088710-0510....................................99, 1088710-0806 ..........................................1088710-1534.............................................958710-1615 ..........................................1088710-1622 ..........................................1088710-1924......................................11, 488710-1930 ......................11, 35, 58, 1088710-1931......................................11, 358710-2699 ..........................................108871700-902 ........................................268871700-906 ........................................268871700-914 ........................................268872700-902 ........................................268872700-906 ........................................268873700-902 ........................................270873700-906 ........................................270


652

PART NUMBER INDEX

873700-932 ........................................270873700-936 ........................................270874700-902 ........................................268874700-906 ........................................268875700-902 ........................................270875700-906 ........................................270875700-932 ........................................270875700-936 ........................................270877150-102 ...............................269, 317877150-106 ...............................269, 317877150-114 ...............................269, 317877250-101 ...............................318, 329877250-102 ...............................269, 317877250-105 ...............................269, 317877250-106 ...............................269, 317877250-112 ...............................269, 317877250-114 ...............................269, 317877952-101 ...............................317, 330877952-102 ...............................283, 317877952-105 ......................283, 317, 330877952-106 ...............................283, 317877952-108 ...............................317, 330877967-102 ...............................273, 318877974-901 ........................................433877974-910 ........................................433878150-101 ...............................282, 318878250-101 ...............................282, 318880668-301 ........................................281880668-901 ........................................281880952-201 ........................................330880952-202 ........................................283880952-203 ........................................334880952-204 ........................................334880952-205 ........................................330880952-206 ........................................283880952-208 ........................................330880952-302 ........................................283880952-701 ........................................330880952-702 ........................................283880952-703 ........................................334880952-704 ........................................334880952-705 ........................................330880952-706 ........................................283880952-708 ........................................330880952-710 ........................................283880952-712 ........................................283880952-714 ........................................334880967-201 ...............................267, 273880967-202 ........................................273880967-302 ........................................273880967-901 ........................................273880967-902 ........................................273880975-201 ........................................329880975-202 ........................................267880975-205 ........................................267880975-209 ........................................267880975-212 ........................................267880975-302 ........................................267880975-305 ........................................267880975-306 ........................................267880975-309 ........................................267880975-312 ........................................267880975-314 ........................................267880975-901 ........................................329880975-902 ........................................267880975-905 ........................................267880975-906 ........................................267880975-909 ........................................267880975-912 ........................................267880975-914 ........................................267880995-202 ........................................372880995-205 ........................................372

880995-206 ........................................372880995-209 ........................................372880995-902 ........................................372880995-905 ........................................372880995-906 ........................................372880995-909 ........................................372881750-902 ........................................372883668-301 ........................................281883668-901 ........................................281883700-704 ........................................334883700-714 ........................................334883700-901 ........................................329883700-902 ........................................273883700-905 ........................................268883700-906 ........................................268883700-909 ........................................268883700-912 ........................................268883700-922 ........................................268883725-901 ........................................281883750-902 ........................................372883750-905 ........................................372883750-906 ........................................372883750-909 ........................................372883952-302 ........................................283883952-701 ........................................330883952-702 ........................................283883952-703 ........................................334883952-704 ........................................334883952-705 ........................................330883952-706 ........................................283883952-708 ........................................330883952-710 ........................................283883952-712 ........................................283883952-714 ........................................334883967-302 ........................................273883967-901 ........................................273883967-902 ........................................273883975-202 ........................................267883975-302 ........................................267883975-305 ........................................267883975-306 ........................................267883975-309 ........................................267883975-312 ........................................267883975-314 ........................................267883975-901 ........................................329883975-902 ........................................267883975-905 ........................................267883975-906 ........................................267883975-909 ........................................267883975-912 ........................................267883975-914 ........................................267883995-902 ...............................210, 372883995-905 ........................................372883995-906 ........................................372883995-909 ........................................372884950-507 ........................................283884950-526 ........................................283884950-543 ........................................283884950-567 ........................................267884950-577 ........................................281884973-701 ........................................433884973-901 ........................................433884973-902 ........................................433884975-202 ........................................267895050-902 ......................317, 373, 466895050-906 ......................317, 373, 466895050-909 ......................317, 373, 466895100-902 ......................317, 373, 466895100-906 ......................317, 373, 466895100-909 ......................317, 373, 466895150-902 ......................317, 373, 466895150-906 ......................317, 373, 466

895150-909 ......................317, 373, 466897150-102 ......................317, 373, 466897150-106 ......................317, 373, 466897150-109 ......................317, 373, 466897250-102 ......................317, 373, 466897250-105 ......................317, 373, 466897250-106 ......................317, 373, 466897250-109 ......................317, 373, 466921700-902 ...............................245, 263921700-932 ...............................245, 263921975-902 ...............................245, 263921975-932 ...............................245, 263922700-902 ...............................245, 262922700-932 ...............................245, 262922975-902 ......................243, 245, 262922975-906 ...............................245, 262922975-932 ...............................245, 262923700-902 ...............................245, 263923700-932 ...............................245, 263923975-902 ...............................245, 262923975-932 ...............................245, 262924700-902 ...............................243, 261924700-906 ...............................243, 261924975-302 ...............................243, 260924975-306 ...............................243, 260924975-902 ...............................243, 260924975-906 ...............................243, 260925700-902 ...............................245, 263925700-932 ...............................245, 263925975-902 ...............................245, 262925975-932 ...............................245, 262926700-902 ...............................243, 261926700-906 ...............................243, 261926975-302 ...............................243, 260926975-306 ...............................243, 260926975-902 ...............................243, 260926975-906 ...............................243, 260927700-902 ...............................243, 261927700-906 ...............................243, 261927975-302 ...............................243, 260927975-306 ...............................243, 260927975-902 ...............................243, 260927975-906 ...............................243, 260928700-902 ...............................243, 261928700-906 ...............................243, 261928975-302 ...............................243, 260928975-306 ........................................260928975-902 ...............................243, 260928975-906 ........................................2609300-1747 ..........................................1999300-1748 ..........................................1999301-0407.............................................999301-0656.............................................539301-0722 ..........................................2009301-0895.............................................139301-0978 ..........................................1999301-1291 ..........................................1069301-1337.............................................589301-1420.............................................539301-1421.............................................539301-1446.............................................999301-1450.............................................539301-6341.............................................539301-6342.............................................53930990-902 ........................................260930990-906 ........................................260931975-902 ........................................262931975-906 ........................................262931975-932 ........................................262931975-936 ........................................262932967-902 ........................................260932967-906 ........................................260

933975-902 ........................................262933975-906 ........................................262933975-932 ........................................262933975-936 ........................................262934967-902 ........................................260934967-906 ........................................260935967-902 ........................................260935967-906 ........................................260935967-912 ........................................260946975-902 ........................................260946975-906 ........................................260959701-902 ........................................253959701-906 ........................................253959701-912 ........................................253959701-918 ...............................253, 255959731-902 ...............................243, 253959731-906 ...............................243, 253959731-912 ...............................243, 253959733-902 ........................................253959733-906 ........................................253959733-912 ........................................253959741-902 ...............................243, 253959741-906 ...............................243, 253959741-912 ...............................243, 253959741-918 ......................243, 253, 255959743-901 ........................................325959743-902 ........................................253959743-906 ........................................253959743-912 ........................................253959746-902 ........................................253959746-906 ........................................253959757-301 ...............................238, 325959757-302 ...............................238, 252959757-306 ...............................238, 252959757-312 ........................................238959757-901 ...............................238, 325959757-902 ......................210, 238, 253959757-906 ...............................238, 253959757-912 ........................................238959758-301 ...............................238, 325959758-302 ...............................238, 252959758-306 ...............................238, 252959758-312 ........................................238959758-901 ...............................238, 325959758-902 ...............................238, 253959758-906 ...............................238, 253959758-912 ........................................238959759-302 ...............................238, 252959759-306 ...............................238, 252959759-901 ...............................238, 325959759-902 ...............................238, 253959759-906 ...............................238, 253959759-912 ........................................238959763-902 ........................................253959763-906 ........................................253959763-912 ........................................253959764-902 ...............................243, 253959764-906 ...............................243, 253959764-912 ...............................243, 253959764-918 ......................243, 253, 255959790-918 ...............................253, 255959793-901 ........................................325959793-902 ........................................253959793-906 ........................................253959793-912 ........................................253959793-918 ...............................253, 255959794-902 ........................................243959931-902 ...............................243, 252959931-906 ...............................243, 252959931-912 ...............................243, 252959931-918 ......................243, 252, 255959933-902 ........................................252

653

PART NUMBER INDEX

959933-906 ........................................252959933-912 ........................................252959936-902 ........................................252959936-906 ........................................252959936-912 ........................................252959941-302 ...............................243, 252959941-306 ...............................243, 252959941-312 ...............................243, 252959941-902 ...............................243, 252959941-906 ...............................243, 252959941-912 ...............................243, 252959941-918 ......................243, 252, 255959943-901 ........................................325959943-902 ........................................252959943-906 ........................................252959943-912 ........................................252959943-918 ...............................252, 255959946-902 ........................................252959946-906 ........................................252959951-902 ...............................243, 252959961-302 ........................................252959961-306 ........................................252959961-312 ........................................252959961-901 ........................................325959961-902 ........................................252959961-906 ........................................252959961-912 ........................................252959961-918 ...............................252, 255959963-302 ........................................252959963-306 ........................................252959963-312 ........................................252959963-902 ...............................210, 252959963-906 ........................................252959963-912 ........................................252959963-918 ...............................252, 255959964-302 ...............................243, 252959964-306 ...............................243, 252959964-312 ...............................243, 252959964-902 ...............................243, 252959964-906 ...............................243, 252959964-912 ...............................243, 252959964-918 ......................243, 252, 255959990-318 ...............................252, 255959990-902 ........................................252959990-906 ........................................252959990-912 ........................................252959990-918 ...............................252, 255959993-302 ........................................252959993-306 ........................................252959993-902 ........................................252959993-906 ........................................252959993-912 ........................................252959993-918 ...............................252, 255959994-902 ........................................243959996-902 ........................................252959996-906 ........................................252959996-912 ........................................252959996-918 ...............................252, 255960967-902 ........................................260960967-905 ........................................260960967-906 ........................................260960967-912 ........................................260961400-302 ........................................394961600-902 ........................................261961600-906 ........................................261961753-902 ........................................261961753-905 ........................................261961753-906 ........................................261961967-302 ........................................260961967-306 ........................................260961967-312 ........................................260961967-902 ........................................260

961967-905 ........................................260961967-906 ........................................260963400-902 ........................................394963600-902 ........................................261963600-906 ........................................261963954-302 ........................................260963954-305 ........................................260963954-306 ........................................260963954-312 ........................................260963967-902 ........................................260963967-905 ........................................260963967-906 ........................................260963967-912 ........................................260965600-902 ........................................261965600-906 ........................................261966400-902 ........................................394966735-902 ........................................261966954-302 ........................................260966967-902 ........................................260966967-905 ........................................260966967-906 ........................................260966967-912 ........................................260970050-902 ...............................261, 318970050-906 ...............................261, 318970100-902 ...............................261, 318970100-906 ...............................261, 318970150-902 ...............................261, 318970150-906 ...............................261, 318971700-902 ........................................261971700-906 ........................................261972700-902 ........................................261972700-906 ........................................261973700-902 ........................................262973700-906 ........................................262973700-932 ........................................262973700-936 ........................................262974700-902 ........................................261974700-906 ........................................261975700-902 ........................................262975700-906 ........................................262975700-932 ........................................262975700-936 ........................................262977150-102 ...............................261, 318977150-106 ...............................261, 318977250-102 ...............................261, 318977250-106 ...............................261, 318981757-302 ...............................238, 260981757-902 ...............................238, 261981758-302 ...............................238, 260981758-902 ...............................238, 261981759-302 ...............................238, 260981759-902 ...............................238, 261990967-202 ........................................260990967-206 ........................................260990967-302 ........................................260990967-305 ........................................260990967-306 ........................................260990967-312 ........................................260990967-902 ........................................260990967-905 ...............................260, 329990967-906 ........................................260990967-912 ........................................260993400-902 ........................................394993700-902 ........................................260993700-905 ...............................260, 329993700-906 ........................................260993700-912 ........................................260993967-302 ........................................260993967-305 ........................................260993967-306 ........................................260993967-312 ........................................260993967-902 ........................................260

993967-905 ...............................260, 329993967-906 ........................................260993967-912 ........................................260A2000020X020..................................301A2000030X020..................................301A2000030X046..................................300A2000050X020..................................301A2000050X030..................................301A2000050X046..................................300A2000100C020..................................302A2000100C030..................................302A2000100C046..................................302A2000100R030..................................302A2000100R046..................................302A2000100T030..................................302A2000100T046..................................302A2000100X020..................................301A2000100X030..................................301A2000100X046..................................300A2000100X212..................................300A2000100X300..................................300A2000125X040..................................301A2000150C046..................................302A2000150R030..................................302A2000150R046..................................302A2000150T030..................................302A2000150T046..................................302A2000150X020..................................301A2000150X030..................................301A2000150X040..................................301A2000150X046..................................300A2000150X212..................................300A2000200X046..................................300A2000250C030..................................302A2000250C046..................................302A2000250R046..................................302A2000250T046..................................302A2000250X020..................................301A2000250X030..................................301A2000250X040..................................301A2000250X046..................................300A2000250X100.........................300, 321A2000250X212.........................300, 321A2000MG...........................................303A2000MG2.........................................303A2001020X020..................................301A2001030X020..................................301A2001030X030..................................301A2001030X046..................................301A2001050C020..................................302A2001050R020..................................302A2001050T020..................................302A2001050X020..................................301A2001050X030..................................301A2001050X046..................................301A2001075X046..................................300A2001100C020..................................302A2001100R030..................................302A2001100R046..................................302A2001100T030..................................302A2001100T046..................................302A2001100X020..................................301A2001100X030..................................301A2001100X046..................................300A2001150C020..................................302A2001150C046..................................302A2001150R020..................................302A2001150R046..................................302A2001150T020..................................302A2001150T046..................................302A2001150X020..................................301A2001150X030..................................301

A2001150X046..................................300A2001200X030..................................301A2001250C046..................................302A2001250X020..................................301A2001250X030..................................301A2001250X046..................................300A2001MG...........................................303A2001MG1.........................................303A2002250X046..................................300A2002250X212.........................300, 321A2002250X500..................................300A2002MG...........................................303A2003020X020.........................301, 332A2003030X020.........................301, 332A2003050X020.........................301, 332A2003050X030.........................301, 332A2003050X046.........................300, 332A2003050X212.........................300, 331A2003100X020.........................301, 332A2003100X030.........................301, 332A2003100X046.........................300, 332A2003125X040.........................301, 332A2003150X020.........................301, 332A2003150X030.........................301, 332A2003150X040.........................301, 332A2003150X046.................300, 331-332A2003250X020.........................301, 332A2003250X030.........................301, 332A2003250X040.........................301, 332A2003250X046.........................300, 332A2003250X212................300, 321, 331A2003MG..................................303, 332A2003MG2................................303, 332A2004250X212................300, 321, 331A2004250X500.........................300, 331A2004MG..................................303, 332A2004MG2................................303, 332A2005020X020.........................301, 332A2005030X020.........................301, 332A2005050X020.........................301, 332A2005050X030.........................301, 332A2005050X046.........................301, 332A2005100X020.........................301, 332A2005100X030.........................301, 332A2005100X046.........................300, 332A2005150X020.........................301, 332A2005150X030.........................301, 332A2005150X046.........................300, 332A2005250X020.........................301, 332A2005250X046.................300-301, 332A2005MG..................................303, 332A2005MG2................................303, 332A2006030X020..................................301A2006050X020..................................301A2006050X046..................................300A2006100X020..................................301A2006100X030..................................301A2006100X046..................................300A2006150X020..................................301A2006150X030..................................301A2006150X046..................................300A2006250X020..................................301A2006250X030..................................301A2006250X046..................................300A2006250X100.........................300, 321A2006250X212..................................300A2006MG...........................................303A2006MG2.........................................303A2007030X020..................................301A2007030X030..................................300A2007050X020..................................301A2007050X030..................................301


654

PART NUMBER INDEX

A2007050X046..................................301A2007100X020..................................301A2007100X030..................................301A2007100X046..................................300A2007150X020..................................301A2007150X030..................................301A2007150X046..................................300A2007250X020..................................301A2007250X030..................................301A2007250X046..................................300A2007MG...........................................303A2007MG2.........................................303A2008250X100..................................300A2008250X212..................................300A2008MG2.........................................303A2010050X020..................................301A2010100X030..................................301A2010100X046..................................300A2010125X040..................................301A2010150X020..................................301A2010150X030..................................301A2010150X040..................................301A2010150X046..................................300A2010250X030..................................301A2010250X040..................................301A2010250X046..................................300A2010250X100..................................321A2010250X212.........................300, 321A2010MG...........................................303A2010MG2.........................................303A2011030X030..................................301A2011050X020..................................301A2011075X046..................................300A2011100X046..................................300A2011150X020..................................301A2011150X046..................................300A2011250X020..................................301A2011MG...........................................303A2011MG2.........................................303A2013020X020.........................301, 332A2013030X020.........................301, 332A2013050X020.........................301, 332A2013050X046.........................300, 332A2013100X020.........................301, 332A2013100X030.........................301, 332A2013100X046.........................300, 332A2013125X040.........................301, 332A2013150X020.........................301, 332A2013150X030.........................301, 332A2013150X040.........................301, 332A2013150X046.........................300, 332A2013250X020.........................301, 332A2013250X030.........................301, 332A2013250X040.........................301, 332A2013250X046.........................300, 332A2013250X100................300, 321, 331A2013250X212................300, 321, 331A2013MG..................................303, 332A2013MG2................................303, 332A2014020X020.........................301, 332A2014030X020.........................301, 332A2014050X020.........................301, 332A2014050X030.........................301, 332A2014050X046.........................301, 332A2014100X020.........................301, 332A2014100X030.........................301, 332A2014100X046.........................300, 332A2014150X020.........................301, 332A2014150X030.........................301, 332A2014150X046.........................300, 332A2014250X020.........................301, 332A2014250X030.........................301, 332

A2014250X046.........................300, 332A2014MG..................................303, 332A2014MG2................................303, 332A2020050X020..................................301A2020050X046..................................300A2020100X030..................................301A2020125X040..................................301A2020150X020..................................301A2020150X030..................................301A2020150X040..................................301A2020150X046..................................300A2020250X020..................................301A2020250X030..................................301A2020250X040..................................301A2020250X046..................................300A2020250X100.........................300, 321A2020250X212..................................300A2020MG...........................................303A2020MG2.........................................303A2021050X020..................................301A2021050X030..................................301A2021050X046..................................301A2021050X100..................................300A2021075X020..................................301A2021100X020..................................301A2021150X020..................................301A2021150X030..................................301A2021250X020..................................301A2021250X046..................................300A2021MG...........................................303A2021MG2.........................................303A2030050X020..................................301A2030100X030..................................301A2030125X040..................................301A2030150X020..................................301A2030150X030..................................301A2030150X040..................................301A2030150X046..................................300A2030250X020..................................301A2030250X030..................................301A2030250X040..................................301A2030250X046..................................300A2030250X100.........................300, 321A2030250X212.........................300, 321A2030MG...........................................303A2031050X020..................................301A2031050X030..................................301A2031050X046..................................301A2031100X020..................................301A2031150X020..................................301A2031250X020..................................301A2031250X046..................................300A2031MG2.........................................303A3000020X020..................................292A3000030X020..................................292A3000050X020..................................292A3000050X046..................................291A3000100C020..................................293A3000100C030..................................293A3000100C046..................................293A3000100R030..................................294A3000100T030..................................294A3000100X020..................................292A3000100X030..................................291A3000100X046..................................291A3000125X040..................................291A3000150C020..................................293A3000150C030..................................293A3000150C046..................................293A3000150R030..................................294A3000150R046..................................294A3000150T030..................................294

A3000150T046..................................294A3000150X020..................................292A3000150X030..................................291A3000150X039..................................291A3000150X046..................................291A3000150X100..................................291A3000150X212..................................292A3000250C020..................................293A3000250C030..................................293A3000250C046..................................293A3000250X020..................................292A3000250X030..................................291A3000250X040..................................291A3000250X046..................................291A3000250X100.........................291, 320A3000250X212..................................292A3000300X039..................................291A3000MG...........................................294A3000MG1.........................................294A3000MG2.........................................294A3001020X020..................................292A3001030X020..................................292A3001030X046..................................291A3001050C020..................................293A3001050C046..................................293A3001050R046..................................294A3001050T046..................................294A3001050X020..................................292A3001050X030..................................292A3001050X046..................................291A3001100C020..................................293A3001100C030..................................293A3001100C046..................................293A3001100R030..................................294A3001100T030..................................294A3001100X020..................................292A3001100X030..................................291A3001100X046..................................291A3001150C020..................................293A3001150C030..................................293A3001150C046..................................293A3001150R030..................................294A3001150T030..................................294A3001150X020..................................292A3001150X030..................................291A3001150X046..................................291A3001250X020..................................292A3001250X030..................................291A3001250X046..................................291A3001MG...........................................294A3001MG2.........................................294A3002100X046..................................291A3002150X046..................................291A3002150X212..................................292A3002250X046..................................291A3002250X100..................................291A3002250X212..................................292A3002250X500..................................292A3002300X039..................................291A3002MG...........................................294A3002MG2.........................................294A3030050X020..................................292A3030100C046..................................293A3030100X020..................................292A3030100X046..................................291A3030150C020..................................293A3030150C046..................................293A3030150R046..................................294A3030150T046..................................294A3030150X020..................................292A3030150X046..................................291A3030250C046..................................293

A3030250X046..................................291A3030250X100.........................291, 320A3030MG...........................................294A3030MG2.........................................294A3031030X020..................................292A3031050R020..................................294A3031050T020..................................294A3031050X020..................................292A3031100C046..................................293A3031100X020..................................292A3031100X046..................................291A3031150C046..................................293A3031150R046..................................294A3031150T046..................................294A3031150X020..................................292A3031150X046..................................291A3031250C046..................................293A3031250X046..................................291A3031MG...........................................294A3031MG2.........................................294A3032100X046..................................291A3032150X046..................................291A3032250X046..................................291A3032250X100.........................291, 320A3032250X212.........................292, 320A3032250X500..................................292A3040030X020..................................292A3040050X020..................................292A3040050X046..................................291A3040100X020..................................292A3040100X046..................................291A3040100X212..................................292A3040150X020..................................292A3040150X030..................................291A3040150X046..................................291A3040250X030..................................291A3040250X046..................................291A3040250X100..................................320A3040MG...........................................294A3040MG1.........................................294A3040MG2.........................................294A3041020X020..................................292A3041030X020..................................292A3041050X020..................................292A3041050X030..................................292A3041050X046..................................291A3041100X020..................................292A3041100X030..................................291A3041100X046..................................291A3041150X020..................................292A3041150X030..................................291A3041150X046..................................291A3041200X020..................................292A3041250X020..................................292A3041250X046..................................291A3041MG...........................................294A3041MG1.........................................294A3041MG2.........................................294A3050020X020..................................292A3050030X020..................................292A3050050X020..................................292A3050050X046..................................291A3050100X020..................................292A3050100X030..................................291A3050100X046..................................291A3050150X030..................................291A3050150X046..................................291A3050150X100..................................291A3050150X212..................................292A3050250X046..................................291A3050250X100.........................291, 320A3050250X212..................................292

655

PART NUMBER INDEX

A3050MG...........................................294A3050MG2.........................................294A3051020X020..................................292A3051030X020..................................292A3051050X020..................................292A3051050X030..................................292A3051050X046..................................291A3051100X020..................................292A3051100X030..................................291A3051100X046..................................291A3051150X020..................................292A3051150X030..................................291A3051150X046..................................291A3051250X046..................................291A3051MG...........................................294A3051MG2.........................................294A6000030X020..................................296A6000030X212..................................296A6000050X020..................................296A6000050X046..................................295A6000050X100..................................295A6000050X212.........................296, 320A6000050X300..................................296A6000100X020..................................296A6000100X030..................................295A6000100X046..................................295A6000100X212.........................296, 320A6000100X300.........................296, 320A6000150X020..................................296A6000150X030..................................295A6000150X040..................................295A6000150X046..................................295A6000150X100..................................295A6000150X212.........................296, 320A6000150X300.........................296, 320A6000250X020..................................296A6000250X030..................................295A6000250X040..................................295A6000250X046..................................295A6000250X100..................................295A6000250X212.........................296, 320A6000250X300.........................296, 320A6000MG...........................................297A6000MG2.........................................297A6001020X020..................................296A6001030X030..................................295A6001030X046..................................295A6001050X020..................................296A6001050X030..................................295A6001050X046..................................295A6001100X010..................................296A6001100X020..................................296A6001100X030..................................295A6001100X046..................................295A6001150X010..................................296A6001150X020..................................296A6001150X030..................................295A6001150X046..................................295A6001250X020..................................296A6001250X046..................................295A6001MG...........................................297A6001MG2.........................................297A6002050X046S ...............................295A6002150X300..................................320A6002250X046..................................295A6002250X100.........................295, 320A6002250X212.........................296, 320A6002250X300..................................320A6002250X500.........................296, 320A6002MG...........................................297A6004250X046.........................295, 331A6004250X100.........................295, 331

A6004250X212................296, 320, 331A6004250X300................296, 320, 331A6004250X500................296, 320, 331A6004MG...........................................297A6005050X020.........................296, 331A6005050X046.........................295, 331A6005100X046.........................295, 331A6006050X046.........................295, 331A6006100X021.........................296, 331A6006100X046.........................295, 331A6010050X020..................................296A6010100X020..................................296A6010100X030..................................295A6010100X046..................................295A6010100X212..................................320A6010150X020..................................296A6010150X030..................................295A6010150X040..................................295A6010150X046..................................295A6010150X212..................................320A6010250X030..................................295A6010250X040..................................295A6010250X046..................................295A6010250X300..................................320A6010MG...........................................297A6010MG2.........................................297A6011050X020..................................296A6011050X030..................................295A6011050X046..................................295A6011100X020..................................296A6011100X030..................................295A6011100X046..................................295A6011150X020..................................296A6011150X030..................................295A6011MG...........................................297A6011MG2.........................................297A6012250X212..................................296A6020050X020..................................296A6020050X046..................................295A6020100X030..................................295A6020100X046..................................295A6020100X212.........................296, 320A6020150X020..................................296A6020150X030..................................295A6020150X046..................................295A6020150X300..................................296A6020250X020..................................296A6020250X030..................................295A6020250X046..................................295A6020250X100..................................295A6020250X212.........................296, 320A6020MG...........................................297A6020MG2.........................................297A6021030X020..................................296A6021030X046..................................295A6021050X020..................................296A6021050X030..................................295A6021050X046..................................295A6021100X010..................................296A6021100X020..................................296A6021100X030..................................295A6021100X046..................................295A6021150X020..................................296A6021150X030..................................295A6021150X046..................................295A6021150X100..................................295A6021250X020..................................296A6021250X046..................................295A6021MG...........................................297A6021MG2.........................................297A6022250X500..................................320A7000100C030..................................293

A7000100R030..................................294A7000100T030..................................294A7000150C046..................................293A7000150R046..................................294A7000150T046..................................294A7000150X046..................................291A7000250C046..................................293A7000250R046..................................294A7000250T046..................................294A7000250X046..................................291A7000MG3.........................................297A7001100C046..................................293A7001100R030..................................294A7001100R046..................................294A7001100T030..................................294A7001100T046..................................294A7001100X020..................................292A7001100X030..................................291A7001100X046..................................291A7001150C046..................................293A7001150R046..................................294A7001150T046..................................294A7001MG3.........................................297A7501030X020..................................297A7501050X020..................................297A7501100X020..................................297A7501100X030..................................297A7501150X020..................................297A7501150X030..................................297A7511030X020..................................297A7511050X020..................................297A7511100X020..................................297A7511150X030..................................297A7521030X020..................................297A7521050X020..................................297A7521100X020..................................297BHT-4 .........................................104, 108BMT-4 .................................................108G1103-60001........................................90G1156-68711........................................83G1156-68712........................................83G1156-68713........................................83G1156-68714........................................83G1160-68706........................................83G1310-68730........................................59G1310-68731........................................59G1310-68741........................................59G1310-68742........................................59G1311-60003........................................53G1311-60006........................................12G1311-60009........................................48G1311-68705........................................60G1311-68710........................................59G1311-68711........................................59G1312-60020........................................49G1312-60025........................................49G1312-60061........................................48G1312-60066........................................49G1312-60067........................................49G1312-67305........................................23G1312-67500........................................23G1312-68711........................................59G1312-68716........................................53G1312-68726........................................60G1312-68730........................................60G1312-68741........................................59G1312-68755........................................60G1312-87303........................................23G1312-87304........................................23G1312-87305........................................28G1312-87306........................................28G1312-87330........................................54

G1313-27302........................................65G1313-43204........................................63G1313-43216........................................35G1313-44510........................................65G1313-44512........................................65G1313-44513........................................65G1313-60004........................................65G1313-68709........................................66G1313-68711........................................67G1313-68719........................................66G1313-68730........................................66G1313-87102........................................62G1313-87201........................................62G1313-87202........................................62G1313-87203........................................62G1313-87300........................................34G1313-87303.................................32, 64G1313-87304.................................23, 82G1313-87305 ..........................23, 33, 82G1314-60081..................................91-92G1314-60082..................................91-92G1314-60083..................................91-92G1314-60086..................................91-92G1314-60087..................................91-92G1314-60100........................................90G1314-60101........................................90G1314-60182..................................91-92G1314-60183..................................91-92G1314-60186..................................91-92G1314-60187..................................91-92G1314-65052.................................91, 97G1314-65054.................................91, 97G1314-65056........................................97G1314-65061.................................91, 97G1314-87301........................................92G1314-87302........................................92G1315-27705........................................96G1315-45003.................................11, 95G1315-60011..................................94-95G1315-60012..................................94-95G1315-60015..................................94-95G1315-60016.................................94, 96G1315-60017.................................94, 96G1315-60018.................................94, 96G1315-60022..................................94-95G1315-60024..................................94-95G1315-60025..................................94-95G1315-67301........................................96G1315-67302........................................96G1315-68703........................................31G1315-68708..................................31-32G1315-68712........................................97G1315-68713.................................91, 97G1315-68715..................................96-97G1315-68716.................................94, 96G1315-68724.................................94, 96G1315-68725..................................96-97G1315-80001........................................96G1315-80002........................................96G1315-80003........................................96G1315-80004........................................96G1315-87101........................................96G1315-87302........................................95G1315-87303........................................23G1315-87305........................................96G1315-87306........................................95G1315-87311 ...................23, 33, 92, 99G1315-87312........................................23G1315-87313........................................96G1315-87318........................................96G1315-87319........................................95G1315-87321........................................95


656

PART NUMBER INDEX

G1315-87323........................................96G1315-87325........................................95G1315-87328........................................96G1315-87333........................................96G1315-87338........................................96G1315-87339........................................95G1316-27301........................................28G1316-60001........................................82G1316-67005........................................75G1316-67006........................................75G1316-67007........................................75G1316-67009........................................75G1316-68708........................................83G1316-68710........................................83G1316-68711........................................83G1316-68716.................................38, 82G1316-68721........................................83G1316-68744........................................82G1316-80002........................................82G1316-80003........................................82G1316-80004........................................82G1316-83200........................................82G1316-87300 ..........................23, 33, 82G1316-87303.................................27, 82G1316-87305........................................27G1316-87306........................................28G1316-87309........................................23G1316-87312........................................27G1316-87313........................................27G1316-87314........................................27G1316-87316........................................27G1316-87317........................................27G1316-87318........................................27G1316-87319........................................27G1316-87321........................................28G1316-87323........................................28G1321-60005........................................99G1321-60007........................................99G1321-60015........................................99G1322-67300........................................58G1322-68705.................................58, 60G1328-87600........................................23G1329-60011........................................65G1329-68718........................................67G1329-68727........................................67G1329-68736........................................67G1329-68737........................................67G1329-80001........................................62G1329-87012........................................62G1329-87017........................................62G1329-87101........................................62G1329-87103........................................62G1329-87300........................................23G1329-87302.................................32, 64G1353-68750........................................75G1361-22402........................................50G1361-23204........................................54G1361-23205........................................54G1361-60012........................................49G1361-60022........................................53G1361-67302........................................26G1361-68707........................................60G1361-68710........................................60G1362-68706........................................98G1362-68709........................................98G1362-87300........................................98G1362-87301........................................98G1364-27107........................................71G1364-60021........................................71G1364-68706........................................71G1364-68711........................................70G1364-68712........................................70

G1364-68723........................................70G1364-81701........................................71G1364-83205........................................71G1364-84516........................................69G1364-84521........................................69G1364-84522........................................69G1364-84523........................................69G1364-84524........................................69G1364-84525........................................69G1364-84531........................................69G1364-84532........................................69G1364-86711........................................71G1364-87201........................................70G1364-87202........................................70G1364-87304..................................70-71G1364-87305..................................70-71G1364-87306..................................70-71G1367-60001........................................69G1367-68730........................................66G1367-68734........................................66G1367-68741........................................66G1367-87012........................................63G1367-87017........................................63G1367-87101........................................62G1367-87102........................................62G1367-87200.................................62, 70G1367-87201........................................62G1367-87202........................................63G1367-87300.................................32, 64G1367-87304........................................28G1375-87301........................................31G1375-87302........................................31G1375-87303.................................32, 64G1375-87304........................................31G1375-87305........................................32G1375-87306........................................32G1375-87308........................................32G1375-87309..................................31-32G1375-87310........................................31G1375-87311........................................32G1375-87312........................................32G1375-87315.................................32, 64G1375-87320........................................31G1375-87321........................................31G1375-87322........................................31G1375-87323........................................31G1375-87324........................................31G1375-87325........................................31G1375-87326........................................34G1375-87327........................................31G1376-60003........................................53G1376-60005........................................59G1376-68705........................................60G1376-68707........................................60G1376-68710........................................60G1377-44900........................................63G1377-87000........................................63G1377-87001........................................63G1377-87002........................................63G1377-87201........................................63G1377-87300.................................32, 64G1377-87310.................................32, 64G1379-67310........................................58G1600-23223 .....................................199G1600-60002 .....................................190G1600-60007 .....................................199G1600-60013 .....................................194G1600-60027 .....................................192G1600-60033 .....................................199G1600-60132 .....................................180G1600-60150 .....................................190G1600-60210 .....................................190

G1600-60211 .....................................178G1600-60230 .....................................190G1600-60232 .....................................180G1600-60233 .....................................180G1600-60310 .....................................190G1600-60311 .....................................178G1600-60330 .....................................190G1600-60332 .....................................180G1600-60400 .....................................194G1600-60411 .....................................178G1600-60419 .....................................184G1600-61132 .....................................180G1600-61211 .....................................178G1600-61219 .....................................184G1600-61232 ............................173, 180G1600-61239 .....................................184G1600-61311 .....................................178G1600-61332 .....................................180G1600-61411 .....................................178G1600-61419 .....................................184G1600-62132 .....................................180G1600-62211 ............................172, 178G1600-62232 .....................................180G1600-62311 ............................174, 178G1600-62318 .....................................185G1600-62332 .....................................180G1600-62402 .....................................199G1600-62411 .....................................178G1600-62700 .....................................190G1600-63200 .....................................192G1600-63211 .....................................178G1600-63311 .....................................178G1600-63411 .....................................178G1600-64211 ............................175, 178G1600-64232 .....................................180G1600-64311 .....................................178G1600-64332 .....................................180G1600-64411 .....................................178G1600-67201 .....................................199G1600-67219 ............................184, 195G1600-67220 .....................................195G1600-67311 .............................194-195G1600-67312 .....................................195G1600-67319 ............................184, 195G1600-68319 ............................184, 192G1600-68714 .....................................192G1600-68715 .....................................192G1600-68716 .....................................192G1600-68723 .....................................192G1603A...............................................194G1607-20030 .....................................195G1607-60000 .....................................195G1607-60001 .....................................195G1607-60041 .....................................195G1607A...............................................195G160U-60419.....................................184G160U-61219.....................................184G160U-61239.....................................184G160U-61419.....................................184G1946-00034 .....................................107G1946-20215 .....................................108G1946-20301 .....................................105G1946-60037 .....................................105G1946-60098 .....................................105G1946-60157 .....................................108G1946-60180 .....................................108G1946-80009 .....................................105G1946-80019 .....................................106G1946-80049 .....................................108G1946-80054 .....................................108G1946-85004 .....................................107G1946-85021 .....................................107

G1947-20029 .....................................105G1947-60103 .....................................105G1956-20302 .....................................106G1956-80000 .....................................106G1958-60098 .....................................105G1958-60136 .....................................105G1960-80039 .....................................107G1960-80060 .....................................105G1969-20302 .....................................106G1969-60086 .....................................108G1969-85000 .....................................110G1969-85001 .....................................107G1969-85003...............................15, 107G1969-85010 .....................................110G1969-85020 .....................................110G1969-85026 .....................................107G1972-60025........................................71G1978-85000...............................15, 107G1982-85001........................................15G1982-85002........................................15G1982-85003........................................15G2228-68700........................................59G2250-04500........................................65G2250-04501........................................65G2250-04502........................................65G2250-04503........................................65G2250-04504........................................65G2255-68700.................................65, 69G2255-68709........................................65G2255-68710........................................65G2255-68720........................................65G2255-68730........................................65G2258-23201........................................54G2258-60003........................................64G2258-60011........................................65G2258-68710........................................63G2258-87102........................................63G2258-87307........................................34G2258-87310........................................34G2258-87311........................................34G2258-87312........................................34G2258-87313........................................34G2258-87314........................................34G2258-87315........................................34G2258-87316........................................34G2260-68711.................................32, 64G2260-87101........................................63G2260-87201........................................63G2260-87300........................................26G2260-87301........................................26G2421-60001 .....................................110G2423A...............................................107G2424A...............................................107G2425A...............................................107G2426A...............................................107G2427A...............................................105G2428A...............................................105G2431A...............................................110G2432A...............................................110G2441-80010 .....................................106G2453-85050 .....................................107G2453-85060 .....................................107G2455-85001........................................15G2571-80103 .....................................106G3199B...............................................109G4203-68708........................................11G4204-40000........................................51G4204-40005........................................51G4204-60004........................................51G4204-60022........................................49G4208-68700........................................11G4212-60007........................................94

657

PART NUMBER INDEX

G4212-60008........................................94G4212-60011........................................94G4212-60022........................................51G4212-60032........................................94G4212-60038........................................94G4212-68001........................................51G4216-68711........................................67G4218-20000........................................98G4218-20001........................................98G4218-20002........................................98G4218-20003........................................98G4218-20004........................................98G4218-40000........................................98G4218-40010........................................98G4218-40011........................................98G4218-40100........................................98G4218-40110........................................98G4218-40130........................................98G4218-40150........................................98G4218-40220........................................98G4218-60100........................................98G4218-68010........................................98G4218-85000.................................15, 98G4220-20012........................................11G4220-24013........................................52G4220-26210........................................52G4220-60006........................................51G4220-60007........................................53G4220-60012........................................51G4220-60015........................................51G4220-60016........................................51G4220-60022........................................49G4220-60028........................................49G4220-60035........................................51G4220-63010........................................52G4220-63015........................................52G4226-60021........................................65G4226-60310.................................32, 64G4226-67001........................................67G4226-68735........................................66G4226-87012........................................63G4226-87020........................................63G4226-87201........................................63G4240-23705 .....................................100G4240-25206 .....................................100G4240-43200 .....................................100G4240-87300 .....................................100G4240-87301 .....................................100G4240-87302 .....................................100G4240-87303 .....................................100G4240-87304 .....................................100G4240-87309 .....................................100G4240-87310 .....................................100G4280-60031........................................48G4280-60033........................................48G4280-60061........................................48G4280-68710.................................60, 66G4280-68730.................................60, 66G4280-68750.................................60, 66G4280-68770.................................60, 66G4296-68715........................................11G5611-21503................51, 64, 101-102G5611-26210...............................52, 101G5611-60020...............................49, 101G5611-60025...............................49, 101G5611-60061...............................48, 101G5611-60067...............................49, 101G5611-60500........................................30G5611-60501........................................30G5611-60502........................................30G5611-60503........................................30G5611-63010 .....................................101

G5611-67300........................................30G5611-67301........................................30G5611-68710........................................37G5611-68741...............................59, 101G5615-60005 .....................................102G5615-60017 .....................................102G5615-60018 .....................................102G5615-60022 .....................................102G5616-60050...............................30, 102G5664-86703 .....................................102G5664-86706 .....................................102G5667-40500 .....................................102G5667-60310........................................32G5667-60320...............................64, 102G5667-60500........................................30G5667-60501........................................30G5667-60502........................................30G5667-60503........................................30G5667-60504........................................30G5667-60505........................................30G5667-87017...............................63, 102G5667-87200...............................63, 101G6011A...............................................109G6012A...............................................109G6013A...............................................109G6014A...............................................109G7100-60002 .....................................190G7100-60007 .....................................199G7100-60033 .....................................199G7100-60150 .....................................190G7100-60210 .....................................190G7100-60230 .....................................190G7100-60310 .....................................190G7100-60330 .....................................190G7100-60400 ............................190, 194G7100-62700 .....................................190G7100-68705 .....................................200G7100-68723 .....................................192PCG931AAKIT...................................322PCG932AAKIT...................................322PCG933AAKIT...................................322PCG93LL500X25...............................322PCG93LL500X25WJ ........................322PCG93LL500X50...............................322PCG93LL500X50WJ ........................322PCG93LL500X75...............................322PCG93LL500X75WJ ........................322PCG93LLSTAND123 ........................322PL1012-5A05.....................................475PL1013-2100......................................511PL1013-2120......................................511PL1013-2300......................................511PL1013-2500......................................511PL1020-2830......................................511PL1049-2800......................................511PL1110-1120.............................500, 502PL1110-1220.............................500, 502PL1110-1320......................................500PL1110-1400......................................508PL1110-1520......................................500PL1110-6100......................................500PL1110-6100LS.................................502PL1110-6115......................................505PL1110-6120......................................505PL1110-6125......................................505PL1110-6130......................................505PL1110-6140......................................505PL1110-6150......................................505PL1110-6160......................................505PL1110-6200......................................500PL1110-6200LS.................................502PL1110-6300......................................500

PL1110-6320......................................505PL1110-6400......................................508PL1110-6500......................................500PL1110-6504......................................500PL1110-6515......................................505PL1110-6520......................................505PL1110-6525......................................505PL1110-6530......................................505PL1110-6540......................................505PL1110-6550......................................505PL1111-3500.............................310, 393PL1113-1300......................................518PL1113-1320......................................521PL1113-1325......................................520PL1113-1500......................................516PL1113-3100......................................511PL1113-3120......................................511PL1113-3300......................................511PL1113-3500......................................511PL1113-6300......................................518PL1113-6325......................................520PL1113-6500......................................516PL1113-6520......................................521PL1114-1900HFIP.............................509PL1114-6900HFIP.............................509PL1117-1800......................................512PL1117-1830......................................512PL1117-6800......................................512PL1117-6830......................................512PL1120-3830......................................511PL1120-6520......................................525PL1120-6830......................................525PL1145-1802......................................474PL1145-1803......................................474PL1147-1501......................................428PL1147-6501......................................428PL1149-1530......................................525PL1149-1840......................................525PL1149-3800......................................511PL1149-6240......................................525PL1149-6250......................................525PL1149-6260......................................525PL1149-6800......................................525PL1149-6801......................................525PL1149-6820......................................525PL1149-6840......................................525PL1149-6850......................................525PL1149-6860......................................525PL1151-1802......................................474PL1151-1803......................................474PL1151-3802......................................474PL1151-3803......................................474PL1170-1810......................................342PL1170-1820......................................342PL1170-1830......................................342PL1170-1840......................................342PL1170-1850......................................342PL1170-1860......................................342PL1170-2820......................................342PL1170-2823......................................342PL1170-6810......................................342PL1170-6820......................................342PL1170-6830......................................342PL1170-6840......................................342PL1170-6860......................................342PL1171-1140......................................342PL1171-6140......................................342PL1210-1120......................................506PL1210-3120EPA..............................507PL1210-6100......................................506PL1210-6104......................................506PL1210-6115......................................506

PL1210-6120......................................506PL1210-6120EPA..............................507PL1210-6125......................................506PL1210-6130......................................506PL1210-6140......................................506PL1210-6150......................................506PL1210-6160......................................506PL1212-1102......................................470PL1212-1103......................................470PL1212-3100......................................470PL1212-3101......................................470PL1212-3702......................................470PL1212-3703......................................470PL1212-3800......................................470PL1212-3801......................................470PL1212-6100......................................470PL1212-6101......................................470PL1212-6200......................................470PL1212-6201......................................470PL1212-6400......................................470PL1212-6401......................................470PL1212-6800......................................470PL1212-6801......................................470PL1213-6520......................................521PL1220-6130......................................528PL1245-1102......................................474PL1245-1103.............................411, 474PL1245-3102......................................474PL1245-3103.............................411, 474PL1245-3702.............................411, 474PL1245-3703.............................411, 474PL1249-1120.............................525, 528PL1249-6100......................................528PL1249-6140......................................528PL1249-6150......................................528PL1251-1102.............................409, 474PL1251-1103.............................409, 474PL1251-3102.............................409, 474PL1251-3103.............................409, 474PL1251-3702.............................409, 474PL1251-3703.............................409, 474PL1310-0001......................................529PL1310-0002......................................529PL1310-0005......................................529PL1310-0007......................................529PL1310-0008......................................529PL1310-0012......................................529PL1310-0016....................310, 342, 393PL1310-0036......................................529PL1310-0048......................................529PL1312-1300.............................393, 463PL1312-1301......................................463PL1312-1500.............................393, 463PL1312-1501......................................463PL1312-1502.............................393, 463PL1312-1503......................................463PL1312-1802.............................393, 463PL1312-1803......................................463PL1312-3300.............................393, 463PL1345-1502.............................411, 463PL1345-1503.............................411, 463PL1351-1502.............................409, 463PL1351-1503.............................409, 463PL1410-0101......................................529PL1410-0200......................................529PL1410-0301......................................529PL1410-0501......................................529PL1412-4100......................................471PL1412-4101......................................471PL1412-4102......................................471PL1412-4103......................................471PL1412-4200......................................471


658

PART NUMBER INDEX

PL1412-4201......................................471PL1412-4400......................................471PL1412-4401......................................471PL1412-4702......................................471PL1412-4703......................................471PL1412-4A05.....................................475PL1412-4K00 .....................................471PL1412-4K01 .....................................471PL1412-4K02 .....................................471PL1412-6100......................................471PL1412-6101......................................471PL1412-6102......................................471PL1412-6103......................................471PL1412-6200......................................471PL1412-6201......................................471PL1412-6400......................................471PL1412-6401......................................471PL1412-6702......................................471PL1412-6703......................................471PL1412-6800......................................471PL1412-6801......................................471PL1412-6A05.....................................475PL1412-6K00 .....................................471PL1412-6K01 .....................................471PL1412-6K02 .....................................471PL1417-0800......................................512PL1417-0830......................................512PL1445-4102.............................411, 474PL1445-4103......................................474PL1445-4702.............................411, 474PL1445-4703.............................411, 474PL1445-6102.............................411, 474PL1445-6103.............................411, 474PL1445-6702.............................411, 474PL1445-6703.............................411, 474PL1451-4102.............................409, 474PL1451-4103.............................409, 474PL1451-4702.............................409, 474PL1451-4703.............................409, 474PL1451-6102.............................409, 474PL1451-6103.............................409, 474PL1451-6702.............................409, 474PL1451-6703.............................409, 474PL1510-1100......................................504PL1510-1200......................................504PL1510-1300......................................504PL1510-1500......................................504PL1510-1504......................................504PL1510-5100......................................504PL1510-5200......................................504PL1510-5300......................................504PL1510-5500......................................504PL1510-5504......................................504PL1512-1300.............................310, 393PL1512-1301.............................310, 393PL1512-1500.............................310, 393PL1512-1501.............................310, 393PL1512-1502.............................310, 393PL1512-1503.............................310, 393PL1512-1801.............................310, 393PL1512-1802.............................310, 393PL1512-1803.............................310, 393PL1512-3100......................................470PL1512-3101......................................470PL1512-3102......................................470PL1512-3103......................................470PL1512-3200......................................470PL1512-3201......................................470PL1512-3300.............................310, 393PL1512-3301.............................310, 393PL1512-3401......................................470PL1512-3501.............................310, 393

PL1512-3702......................................470PL1512-3703......................................470PL1512-3800....................310, 393, 470PL1512-3801....................310, 393, 470PL1512-3802.............................310, 393PL1512-3803.............................310, 393PL1512-5100......................................470PL1512-5101......................................470PL1512-5102......................................470PL1512-5103......................................470PL1512-5200......................................470PL1512-5201......................................470PL1512-5400......................................470PL1512-5401......................................470PL1512-5500.............................310, 393PL1512-5501.............................310, 393PL1512-5702......................................470PL1512-5703......................................470PL1512-5800....................310, 393, 470PL1512-5801....................310, 393, 470PL1512-5802.............................310, 393PL1512-5A05.....................................475PL1514-1900HFIP.............................509PL1514-5900HFIP.............................509PL1545-1502......................................411PL1545-1503......................................411PL1545-1802......................................411PL1545-1803......................................411PL1545-3102.............................411, 474PL1545-3103.............................411, 474PL1545-3702.............................411, 474PL1545-3703.............................411, 474PL1545-3802......................................411PL1545-3803......................................411PL1545-5102.............................411, 474PL1545-5103.............................411, 474PL1545-5702......................................474PL1545-5703.............................411, 474PL1547-1501......................................428PL1547-5501......................................428PL1551-1502......................................409PL1551-1503......................................409PL1551-1802......................................409PL1551-1803......................................409PL1551-3102.............................409, 474PL1551-3103.............................409, 474PL1551-3702.............................409, 474PL1551-3703.............................409, 474PL1551-3802......................................409PL1551-3803......................................409PL1551-5102.............................409, 474PL1551-5103.............................409, 474PL1551-5702.............................409, 474PL1551-5703.............................409, 474PL1570-5810......................................342PL1612-1801.............................310, 393PL1670-0810......................................342PL1670-0820......................................342PL1670-0830......................................342PL1670-0840......................................342PL1670-0850......................................342PL1670-0860......................................342PL1671-0140......................................342PL1712-3100......................................470PL1712-3101......................................470PL1712-3102......................................470PL1712-3103......................................470PL1712-3200......................................470PL1712-3201......................................470PL1712-3400......................................470PL1712-3401......................................470PL1712-3702......................................470

PL1712-3703......................................470PL1712-3800......................................470PL1712-3801......................................470PL1712-6800......................................470PL1712-6801......................................470PL1745-3102......................................474PL1745-3103.............................411, 474PL1745-3702......................................474PL1745-3703.............................411, 474PL1751-3102.............................409, 474PL1751-3103.............................409, 474PL1751-3702.............................409, 474PL1751-3703.............................409, 474PL1812-3102......................................470PL1812-3103......................................470PL1812-6100......................................470PL1812-6101......................................470PL1812-6200......................................470PL1812-6201......................................470PL1812-6400......................................470PL1812-6401......................................470PL1812-6800......................................470PL1812-6801......................................470PL1845-2102......................................474PL1845-2103.............................411, 474PL1845-3102.............................411, 474PL1845-3103.............................411, 474PL1851-2102.............................409, 474PL1851-2103.............................409, 474PL1851-3102.............................409, 474PL1851-3103.............................409, 474PL1912-1300.............................310, 393PL1912-1301.............................310, 393PL1912-1500.............................310, 393PL1912-1501.............................310, 393PL1912-1502.............................310, 393PL1912-1503.............................310, 393PL1912-1801.............................310, 393PL1912-1802.............................310, 393PL1912-1803.............................310, 393PL1912-3300.............................310, 393PL1912-3301.............................310, 393PL1912-3500.............................310, 393PL1912-3501.............................310, 393PL1912-3801.............................310, 393PL1912-3802.............................310, 393PL1912-3803.............................310, 393PL1912-5500.............................310, 393PL1912-5501.............................310, 393PL1912-5801.............................310, 393PL1945-1502......................................411PL1945-1503......................................411PL1945-1802......................................411PL1945-1803......................................411PL1945-3802......................................411PL1945-3803......................................411PL1951-1502......................................409PL1951-1503......................................409PL1951-1802......................................409PL1951-1803......................................409PL1951-3802......................................409PL1951-3803......................................409PL1C12-2502 .....................................393PL1E10-3120EPA..............................507PL1E10-6120EPA..............................507PL1E12-5A05.....................................475PL1F70-6830......................................342PL1F70-6850......................................342PL2010-0100......................................537PL2010-0101......................................537PL2010-0102......................................537PL2010-0103......................................537

PL2010-0104......................................537PL2010-0105......................................537PL2010-0200......................................535PL2010-0201......................................535PL2010-0202......................................535PL2010-0203......................................535PL2010-0300......................................535PL2010-0301......................................535PL2010-0400......................................535PL2010-0401......................................535PL2010-0402......................................535PL2010-0403......................................535PL2010-0501......................................536PL2010-0505......................................536PL2010-0601......................................536PL2010-0605......................................536PL2012-0001......................................538PL2012-0005......................................538PL2012-0010......................................538PL2012-1001......................................538PL2012-1005......................................538PL2012-1010......................................538PL2012-2001......................................538PL2012-2005......................................538PL2012-2010......................................538PL2012-3001......................................538PL2012-3005......................................538PL2012-3010......................................538PL2012-4001......................................538PL2012-4005......................................538PL2012-4010......................................538PL2012-5001......................................538PL2012-5005......................................538PL2012-5010......................................538PL2012-6001......................................538PL2012-6005......................................538PL2012-6010......................................538PL2012-7001......................................538PL2012-7005......................................538PL2012-7010......................................538PL2012-8001......................................538PL2012-8005......................................538PL2012-8010......................................538PL2012-9001......................................538PL2012-9005......................................538PL2012-9010......................................538PL2013-1001......................................538PL2013-1005......................................538PL2013-1010......................................538PL2013-2001......................................538PL2013-2005......................................538PL2013-2010......................................538PL2013-3001......................................538PL2013-3005......................................538PL2013-3010......................................538PL2013-4001......................................538PL2013-4005......................................538PL2013-4010......................................538PL2013-5001......................................538PL2013-5005......................................538PL2013-5010......................................538PL2013-6001......................................538PL2013-6005......................................538PL2013-6010......................................538PL2013-7001......................................538PL2013-7005......................................538PL2013-7010......................................538PL2013-8001......................................538PL2013-8005......................................538PL2013-8010......................................538PL2013-9001......................................538PL2013-9005......................................538

659

PART NUMBER INDEX




PL2144-2000......................................545PL2144-2001......................................545PL2144-3000......................................545PL2144-3001......................................545PL3540-C603VP................................476PL3540-D603VP................................476PL3540-P603VP................................476PL3549-3603VP ................................476PL3554-1602dAbz ............................347PL3554-1602dCac ............................347PL3554-1602dCbz.............................347PL3554-1602dGdmf .........................347PL3554-1602dGibu...........................347PL3554-1602dT.................................347PL3554-4602dAbz ............................347PL3554-4602dCac ............................347PL3554-4602dCbz.............................347PL3554-4602dGdmf .........................347PL3554-4602dGibu...........................347PL3554-4602dT.................................347RMSN-2..............................................108RMSN-4..............................................108


660

APPLICATION TITLE INDEX

12 phenols analyzed using a longer (4.6 x 100 mm) Agilent Poroshell 120 EC-C18 column.................231

AAdrenocorticosteroids on Pursuit PFP and C18 ..........................................290Agilent Bio SEC-3 column length comparison, 150 mm...................422Agilent Bio SEC-3 column length comparison, 300 mm...................422Alberta Peptide Institute test mix................308, 390Alcohols and aliphatic compounds......................582Alkyd resin..................................................................519Amino acid standard separation on Eclipse Plus C18..................................................564Amitrol in water by LC/MS, 0.05 ppb .................585An overlay of the original ZORBAX Eclipse Plus 5 µm method and Agilent Poroshell 120 method. All 11 peaks on Poroshell 120 are resolved by the time the first peak elutes on the original 5 µmZORBAX Eclipse Plus method ..............................595Analgesics......................................................................618Analgesics: Non-steroidal anti-inflammatory drugs: Narrow bore separation ................................622Analysis of Biocides in Hand Sanitizer ...............580Analysis of Bovine Serum Albumin by lightscattering using ProSEC 300S columns..............429Analysis of carbohydates on Hi-Plex H columns .............................................340Analysis of choline kinase on PL-SAX 4000Å.....407Analysis of ciprofloxacin and ciprofloxacin metabolites................................643Analysis of diazepam on Rx-C18...........................272Analysis of fruit juice...............................................338Analysis of low molecular weight polystyrene and oligomer fractions collected from OligoPore preparative columns ................................522Analysis of oxidized insulin chains.........................553Analysis of pesticide residues in green tea.........594Analysis of representative whey proteins ............408Analysis of sugars with high sodium matrix .......341Analysis of sweeteners on Hi-Plex Ca columns.....340Analysis of water soluble vitamins in multivitamin tablets......................................................612Analytical separation of low molecular weight polystyrene .......................522Anesthetics, local: Bonded phase selectivity....619Anilines, substituted: Rapid separation ..............585Anthocyanins from blueberries: High-efficiency high-speed separation................598Antibiotics: High speed separation ......................620Antibodies: Fast separation of IgM and IgG antibodies ...................................................565Antidepressants, tricyclic: Comparative separation ..........................................636Antifungal medications ...........................................621Antifungals ........................................................290, 621Antihistamines: Fast separations on RRHT Extend-C18 ...............................................617

Antibiotics: Lincomycin and Clindamycin by LC-APCI-MS LC-TIC ............................................620Aromatic acids/benzoic acids: Selectivity differences .............................................623Aromatics II................................................................599Aspartame: Metabolites and applications..........599Aspirin and cough remedy .....................................628

BBSA tryptic digest on RRHT...................................577Barbiturates................................................................643Baseline expansion of a separation of protein standards.................................................414Basic antihistamines on Extend-C18 at high pH.......................................275Benzoic acid/sorbic acid ........................................609Bio-Monolith DEAE column monitors phage production during fermentation................415Blueberry anthocyanin analysis ...........................594Brij 35 ..........................................................................581

CCalibration curves.....................................................505Calibration of the ProSEC 300S column with globular proteins ..............................429Capillary columns for HPLC analyses with UV and MS detection ...................455Carbohydrates in colas............................................601Carbohydrates in juices...........................................601Carbohydrates in milk..............................................602Carbohydrates: Carbohydrate standards.............600Carbohydrates: Effect of mobile phase strength............................600Carbohydrates: Sugar alcohols..............................601Catecholamines.........................................................578Catecholamines/biogenic amines: Rapid separation using ion-pair reagents...........623Charge isoform analysis of monoclonal antibodies.......................................401Chiral ethiazide (diuretic drug) separation .........624Chiral separation of S- and R-Norfluoxetine......626Chiral separation of atenolol..................................627Chiral separation of fluoxetine enantioners (Prozac) ............................624Chiral separation of hexobarbitol..........................625Chiral separation of salbutamol ............................626Chiral separation of tolperison enantiomers .....627Cocaine and metabolites ........................................627Column reproducibility – 200 injections ofreduced monoclonal antibody using an Agilent ZORBAX RRHD 300SB-C3 column........555Column stability testing at pH 3 and 60 °C........257Column stability testing at pH 7.0 ........................258Columns for sample clean-up................................507Comparing HILIC and RPLC of morphine using Agilent ZORBAX RRHD columns with UHPLC/MS ......................................................631Comparison of Aβ peptide RP-HPLC separations at low and high pH............................573

Comparison of Agilent Bio SEC-3 and competitor column in the analysis of a monoclonal antibody.......................................420Comparison of PolyPore with conventional individual pore size GPC columns ...........................................517Comparison of phenols separation with Poroshell 120....................................................584Components of green tea separated on Rapid Resolution StableBond SB-C8.............625Consistent ion-exchange MAb separation ...............................................400, 562Corn syrup, Hi-Plex...................................................339Cough formula mixture: Fast and efficient separation .................................628Cough/cold remedies on ZORBAX 300SCX ......334Crude bradykinin prep load ....................................469Crude peptide screen...............................................476

DDNPH: Derivatized Aldehydes obtained from air.......................................................584Deoxynucleosides: Using rapid resolution 3.5 µm columns.........................................................577Determination of anthocyanins in blueberries .....597Dexamethasone, USP method: Rapid analysis.....639Differences in composition of two alkyl naphthalene sulfonates ........................527Dimethyl-C18/amide, Bonus-RP...........................280

EEasiVial PS-H .............................................................533Eclipse Plus C18 vs. C8 ...........................................250Eclipse Plus C8 is less retentive than Eclipse Plus C18..............................................251Eliminate tailing and maximize resolution with Eclipse Plus Columns.....................................250Environmental phenols on Poroshell 120...........230Epoxy resin ................................................................501Excellent separation of two phenol formaldehyde resins with PolarGel-M.................513Exceptional Lot-to-lot Reproducibility..................426Exceptional separating power ...............................403Exploiting chemical stability – NH4OH concentration....................................308, 390Explosives and related compounds: Qualitative and quantitative analysis...................586Explosives from soil extract ...................................587Extend-C18 provides good peak shape at low pH ....................................................................276

FFast analysis 11 common compounds found in analgesics .................................................615Fast analysis of cefepime and related impurities ....................................217, 611Fast analysis of Pindolol .........................................642Fast analysis of sulfa drugs...................................596Fast and ultra-fast analysis of basic compounds........................................251, 617

Application Title Index

661



Fast LC/MS/MS analysis of group 4pharmaceuticals from EPA 1694 ..........................583Fast method for ginseng analyses scaled from a traditional method.........................612Fast separation of recombinant human erythropoietin..............................................553Fast separation of reduced monoclonal antibody...............................................375Fast vitamin E analysis on Rapid Resolution HT ..........................................608Fast, high-resolution separation of peptides and proteins with Poroshell 300SB-C18 ...............................................572Faster analysis of USP Method for simvastatin tablet...............................................615Faster separation of sulfa drugs ...........................616Faster separations using Agilent weak cation-exchange columns...........................560Fat-soluble vitamins on ZORBAX Eclipse XDB-C8........................................605Five different bonded phases provide selectivity options......................................266Flavoring agents........................................................602Food colors, FD&C....................................................602Four different 300SB bonded phases optimize separation of large polypeptides................................................371Fraction analysis – the concentration overload purification .............469

GGlycosylated proteins: Large Molecules on Poroshell 300SB-C18 and 300SB- ..................565Goldenseal and related alkaloids on Rapid Resolution Eclipse XDB-C18 ......................625Good peak shape over a wide pH range with ZORBAX Eclipse XDB ....................................257Gradient optimizations for ultra-fast analysis of reduced monoclonal antibody .........556Guaifenesin: USP analysis of guaifenesin..........629

HHPLC of 25 bp DNA ladder ..........................307, 388HPLC separation of 12 phenols perfomed in just 5 minutes – and under 400 bar – using an Agilent Poroshell 120 EC-C18 column .............231HSA tryptic digest on ZORBAX Rapid Resolution HT 1.8 µm.................566Heparin........................................................................526Herbicide/pesticide standards: Effect of bonded phase ...........................................588Herbicides on different bonded phases ..............587Herbicides: Rapid separation .................................591High Resolution of 24 Amino Acids Using ZORBAX Eclipse AAA Protocol.................396High purity and high recovery with ZORBAX PrepHT columns ............................315High resolution and fast analysis on RRHT Eclipse PAH column...............................254High resolution normal-phase separation of octylphenoxy ethanol surfactant on ZORBAX CN.........................................................327High resolution separation of a Poly-T-Oligonucleotide size standard spiked with 10-mer, 15-mer, 30-mer and 50-mer (main peaks)........................................408

High sensitivity with capillary columns ..............453Higher resolution of intact monoclonal antibody...368Higher resolution of oxidation study..........354, 368Hormones/steroids..................................................633Human serum: Low abundance protein isolation and identification from 1-D gel band by LC/MS .......................454, 566Hyaluronic acid..........................................................527Hydrophilic purine/pyrimidine separation..........579

IIbuprofen: Optimizing selectivity with RRHT Columns.................................................618Improved peak shape of basic compounds using Bonus-RP .................................279Improved reproducibility of monoclonal antibodies.......................................369Improved resolution with smaller particle size with Agilent weak cation-exchange columns.....559Increase peak capacity with RRHT columns.....240Increased resolution for peptide mapping....357, 369Intact MAb monomer and dimer separation.............................355, 419, 563

LLC/MS analysis of angiotensin on Extend-C18 ...........................................................377LC/MS performance test mix for Polaris C8-A .........................................................299Lamotrigine ................................................................642Large fibrous proteins.....................................309, 392Liquid chromatography phase test mixture (LPTM) on Pursuit C8 ......................290Local anesthetics......................................................619Long life at high pH with 300Extend-C18...........378Long life at high pH with Extend-C18..................275Long lifetime of RRHT columns at elevated temperatures........................................241

MMechanical stability of Pursuit XRs.....................289Metronidazole: Updating USP methods..............629Microbore HPLC for sensitive peptide analysis ...462MicroBore Poroshell 300 columns provide maximum sensitivity for LC/MS............382Mixture of beta blockers ........................................613Monoclonal IgG1 chains: Separation on Poroshell 300SB-C8 .............383, 567Morphine and metabolites: Extracted blood plasma sample separation.......630

NNaproxen analysis ...................................................611Natural products – capsaicin anddihydrocapsaicin on Pursuit XRs C18 .................319Neutraceuticals: Extract from green tea.............603Neutraceuticals: Hypericin separation in St. John's Wort.............632New levels of sensitivity and resolution.............235Nucleosides, purines and pyrimidines ................564Nucleosides: Separation of deoxy and ribonucleosides.................................................568Nucleotides: Separation of mononucleotides ...568

OOligosaccharides.......................................................610Opiates (drugs of abuse) by LC/MS....................630Optimize separations with Eclipse XDB selectivity options.............................259Optimizing protein separations with Agilent weak cation-exchange columns............558Organic acid analysis...............................................338Organic acids separated on ZORBAX SB-Aq.......581Overlay of UV and Light Scattering 90° for aSample of y-globulins, Illustrating Monomer,Dimer, Trimer, and Aggregate Peaks....................430Overlay of UV and light scattering 90° for asample of γ-globulins, illustrating monomer, dimer, and trimer peaks ..........................................430

PpH gradient elution for improved separation of monoclonal antibody charged variants..........561PLgel LS column .......................................................503PLgel Olexis reveals true modalities across the range of polyolefins.............................508Parabens: High speed separation.........................604Peak shape and efficiency are better with ZORBAX Eclipse Plus.....................................249Peptide RP-HPLC/ESI-MS using NH4OH mobile phase yields both positive and negative ion spectra ................................................573Peptides/proteins: Effect of elevated temperature.....................370, 571Peptides/proteins: Equivalent gradient separations............................571Peptides: Effect of TFA concentration........370, 569Peptides: Separation of antiotensins I, II, III with TFA and NH4OH ................................570Peptides: Separation of antiotensins I, II, III with TFA and NH4OH ................................632Phenols, substituted ................................................592Phenoxyacid herbicides ..........................................591Plant hormones: Rapid gradient elution separation.....................................................593Plasticized PVC.........................................................501Polyamides .................................................................509Polycyclic aromatic hydrocarbons according to EPA Method 610...............................589Polyester .....................................................................519Polyesterimide...........................................................520Polyethylene Glycol/Oxide standards .................542Polyethylene glycols .......................................307, 388Polymethylmethacrylate in DMF...........................517Polymethylmethacrylate standards......................540Polyol...........................................................................501Polyphenylene Sulfides...........................................500Polystyrene standards .............................................538Polyurethanes............................................................520Polyvinyl alcohol ..............................................526, 528Pore size choice: Mouse IgG ................................421Pore size choice: Proteins......................................421Poroshell 120 EC-C18 for fast UHPLC separations ..................................................232Poroshell 300 columns separate proteins and peptides in seconds ........................381

662


Preparative fractionation of a culture filtrate containing amyloglucosidases on Agilent PL-SAX 4000Å......................................473Preparative scale purification of Leuprolide by concentration overload.................359Preparative separation of low molecular weight polystyrene ...............................522Protein digest analysis............................................552Protein elution pattern on ZORBAX Poroshell 300SB-C8 ...............................384Proteins in a complex sample by 2-D HPLC with Nano HPLC columns...................457Proteins: Effect of bonded phase .........................575Proteins: Effect of bonded phase, RP..................575Pullulan polysaccharide standards.......................544Purification of a 25-mer trityl-off oligonucleotide and analytical quantitation of the fraction using PLRP-S 100Å, 4.6 x 50 mm ....469Purification of a large oligonucleotide.................473

QQuantification and qualification of vitamin C and citric acid in fresh grapefruit juice ..........................................................609

RRapid analysis of an analgesic tablet, selectivity differences at pH 2.7 and pH 7 .........250Rapid method development for 18 compoundswith an Agilent RRHD Eclipse PAH column......590Rapid Resolution HT (RRHT) provides double the efficiency of Rapid Resolution columns ......240Reduce analysis time dramatically with Rapid Resolution HT columns......................241Reduce peptide map analysis time by 90% with Poroshell 300SB ...............................382Resin analysis by rapid GPC ..................................511Rose wine...................................................................610

SSB-CN optimizes retention and resolution.........266Scale-up from analytical to prep ..........................321Selectivity changes for basic compounds with Eclipse XDB and StableBond.......................258Selectivity comparison of TFA and NH4OH for peptide RP-HPLC\ESI-MS analysis...............574Selectivity comparison of TFA and NHSelectivity comparison: C18 columns............236Selectivity comparison: Phenyl columns ............237Selectivity for urea pesticides ...............................259Selectivity in peptide RP-LC...................................389Selectivity test mix for Polaris columns..............299Separation of 20 PAHs on Eclipse PAH ..............591Separation of 8 steroids .........................................613Separation of azo dye degradation products ....583Separation of Azo Dyes...........................................598Separation of EPA 610 PAH Mix...........................589Separation of a tryptic digest on ZORBAX MicroBore 300SB-C18 .....................461Separation of basic peptides on Bonus-RP versus traditional Alkyl phase ...........569Separation of charge variants of human IgG1 with pH gradient ...............................355

Separation of group 4 analytes in EPA 1694 on ZORBAX HILIC Plus column .........325Separation of heated, stressed MAb...................563Separation of highly basic antidepressants above their pKa in free base form (pKa 9.5-9.7) ...............................................................635Separation of licorice root on RRHD columns ..234Separation of pharmaceutical cardiac drugs.....616Separation of polypeptides in under 1 minute ..572Separation of protein standards on Agilent 3 μm ion-exchange columns by cation-exchange chromatography..................403Separation of recombinant human erythropoietin (rEPO)...............................................562Separation of small molecule anorectics ...........622Separation of vitamin D2/D3.................................605Separation optimization for ultra-fast analysis of reduced and alkylated monoclonal antibody.....554Several ZORBAX RRHD 1.8 µm selectivitiesfacilitate method development .............................614Short-chain ZORBAX 300SB-C3 is stable at low pH, high temperature.................371Shorter chain ZORBAX SB-CN is also stable at low pH (pH 2.0, 50 °C)..............265Space ...........................................................................265Sports drink................................................................610StableBond SB-C18 shows excellent stability at low pH and high temperature...........265Standard ion-exchange protein separation............................................407, 576Standard protein separation ..................................410Standard proteins by reversed-phase..................576Starches......................................................................500Steroids .......................................................................634Steroids: Easy scalability using Agilent Prep columns...................................312Steroids: Separation.................................................633Sub 1 minute separations with RRHD columns.................................................235Sugars..........................................................................604Sugars in plain and milk chocolate......................604Sulfa drugs .................................................................641Sulfonamides – Fast analysis with RRHT columns .................................................640Sunscreen ingredients: Perform conventional, fast and ultra-fast separations on the same column family ............607Superior loadability on Agilent Prep C18 with basic compounds ............................................312

TTemperature as a tool to enhance mass transfer and improve resolution ofoligonucleotides in ion-pair reversed-phase HPLC .....................................391, 579Ten cardiac drugs on Rapid Resolution HT SB-C18 .................................640Theobromine in beverages.....................................608Tocopherols by LC/MS with APPI .......................603Triamcinolone – USP analysis of triamcinolone........................................635Triazine pesticides on Bonus-RP and Alkyl C8 phase...................................................592

Tricyclic antidepressants.........................................636Tricyclic antidepressants and benzodiazepines................................................289Tricyclic antidepressants and metabolites: Effect of pore size ....................637Triton X-114: Decreasing run-time by changing bonded phase ....................................580Two samples of melamine resin analyzed by PolarGel-L ............................................513

UUHPLC efficiency at HPLC pressures ..................230Ultra-high speed and high resolution of intact monoclonal antibodies...........................557USP analysis of tetracyclines ................................639USP method: Glyburide and internal standard, progesterone ...........................................638USP method for sorbitol .........................................341USP methods for sugar alcohols ..........................339Ulcer treatment drugs at intermediate pH .........637Urine, LSD analysis by LC/MS..............................638Use ZORBAX Extend-C18 for alternate selectivity at high pH ....................378, 567

VVX nerve agent metabolites by LC/MS-IS standard (C13 labeled) ........................593Virtually eliminate retention time variations .......400

WWarfarin: USP chromatographic purity method using Eclipse XDB-CN..................640Water-soluble B vitamins separated on ZORBAX SB-Aq ...............................607Water-soluble vitamins ...........................................605Water-soluble vitamins using the USP 23 method ..................................................606Water-soluble vitamins: High speed separation using ion-pairing............606Weak cation-exchange chromatography for P128 therapeutic protein sample on theAgilent 1260 Bio-inert Quaternary LC systemusing different cation-exchange columns..........404Whey proteins in dairy samples – milk......391, 578

XXanthines: Higher resolution, same selectivity with RRHT...................................617

ZZORBAX Bio-SCX Series II provides more retention of small peptides..........................459ZORBAX Bonus-RP is stable at low and mid pH....................................................279ZORBAX Bonus-RP provides unique selectivity.....................................280ZORBAX Eclipse Plus: Best peak shape in the industry without tailing ...............................249ZORBAX Nano columns for high sensitivityprotein digest analysis by LC/MS........................453

663

COMPOUND INDEX


AAcebutolol ..................................................................613Acenaphthene...................................................589-591Acenaphthylene................................................589-591Acephate ....................................................................594Acetaldehyde – DNPH............................................584Acetamide ..................................................................6152-Acetamidophenol.........................................235, 615Acetaminophen.....................235, 250, 615, 618, 628Acetanilide ........................................................235, 618Acetate................................................................174-175Acetic Acid.................................................................581Acetone ......................................................................582Acetone – DNPH......................................................584Acetophenone...........................................................5996-Acetylmorphine .....................................................628Acetylsalicylic acid........................235, 250, 618, 628Acrolein – DNPH......................................................584Adenine..............................................................564, 579Adenosine .........................................................564, 568Adonitol ......................................................................339Adrenaline..................................................................578Alanine...............................................................396, 564Alanine-3-Glycine-4.........................................308, 390Albuterol ............................................................325, 583Alprenolol ...................................................................6132-Amino-5-azotoluene.............................................1834-Aminobenzoic acid ......................................290, 621p-Aminobenzoic acid ...............................................6093-Amino-benzonitrile ...............................................5857-Aminoclonazepam ................................................2892-Amino-4,6-dinitrotoluene ............................586-5874-Amino-2,6-dinitrotoluene ....................................5874-Amino-4,6-dinitrotoluene ....................................5867-Aminoflunitrazepam.............................................2892-Aminonaphthalene ...............................................1832-Amino-4-nitrotoluene...................................586-5872-Amino-6-nitrotoluene...................................586-5874-Amino-2-nitrotoluene...........................................586Amitriptyline ....................................258, 289, 635-637cis-10-OH -Amitriptyline..........................................637trans-10-OH-Amitriptyline.......................................637Ammonium ................................................................173Amylbenzene.............................................................299Amylobarbitone.........................................................643Anadamine.................................................................236Androstadiene 3,17 dione ......................................613Anethole .....................................................................602Angiotensin I .................308, 377, 389-390, 462, 570Angiotensin II ..........................194, 308, 370, 377, 381,

389-390, 462, 570-572Angiotensin III........................308, 377, 389-390, 570Aniline .......................................................183, 583, 598p-Cl-Aniline.................................................................183Anisidine.....................................................................598p-Anisidine .................................................................585

Anthracene ...............................................189, 589-591a-1-Antichymotrypsin.....................................454, 566Antithrombin-III................................................454, 566Apomyoglobin ...........................................................572Aprotinin.....................................................................403Arabinose ...................................................................341Arabitol........................................................................3392-Arachinoylglycerol ................................................381Arginine .............................................................396, 564Arsenate .....................................................................175Arsenite ......................................................................175Ascorbic acid.............................................................612Asparagine ........................................................396, 596Aspartame.......................................232, 290, 299, 599Aspartic acid.....................................................396, 596Aspartic acid-phenylalanine dipeptide................599Atenolol ......................................................................613Atrazine......................................................587-588, 591Azide..........................................................172, 175, 421

BBarberine....................................................................625Barbital........................................................................258Barbitone....................................................................643Beclomethasone.......................................................290Bendroflumethiazide................................................189Bentazon ....................................................................587Benzaldehyde – DNPH ...........................................584Benz(e)pyrene ..........................................................591Benzidine..................................................183, 583, 5981,2-Benzisothiazol-3(2H)-one ................................580Benzisothiiazol-3(2H)-one ......................................235Benzo(a)anthracene .......................................589-591Benzo(a)pyrene.................................................589-591Benzo(b)fluoranthene......................................589-591Benzocaine ................................................................619Benzo(g,h,i)perylene........................................589-591Benzoic acid....................................232, 290, 389, 580,

602, 609, 621, 629Benzo(k)fluoeanthene.....................................589-591Benzophenone ..........................................................618Benzoylecgonine ......................................................627Benzthiazuron ...........................................................588n-6-Benzyl adenine ..................................................5935-Benzyl-3,6-dioxo-2-piperazineacetic acid........599Berberine...........................................................251, 617Biosynthetic human insulin...................................384Biotin (B7)..................................................................612Biphenyl......................................................................189Bovine carbonic anhydrase ..........................407, 576Bromide ......................................................................172BSA...................................382, 425-426, 432, 576-577Bumetanide ...............................................................189Buspirone ...................................................................616Butacaine ..........................................................266, 619tert-butanol ................................................................582

2-Butanone (MEK) – DNPH...................................584Butylbenzene.............................................................299Butylparaben ...........................................189, 241, 604 n-Butyraldehyde – DNPH.......................................584

CCaffeine.........................232, 235, 250, 258, 276, 299,

316, 334, 599, 608, 615Calcium .......................................................................173Calmodulin .................................................................571Canadine.....................................................................625Carbamazepine.................................................618, 632Carbaryl.......................................................................594Carbendazim ............................................235, 580, 594Carbonate...................................................................175Carbonic Anhydrase ......................370-371, 381-382,

408, 571-572Carvone.......................................................................602Catalase ......................................................................432Catechol...................................230-231, 584, 603, 625Cefazolin .....................................................................620Cefepime.....................................................................217Cefotaxime .................................................................620Ceftazidime ................................................................620Celecoxib ....................................................................235Cephaclor ...................................................................280Cephalexin..................................................................280Cephoxitin ..................................................................280Cephuroxime..............................................................280Chlorate.......................................................................172Chloride......................................................172, 174-175Chloroaniline.....................................................583, 598m-Chloroaniline.........................................................585o-Chloroaniline..........................................................585p-Chloroaniline..........................................................5852-Chlorobenzoic ........................................................623Chlorocaine................................................................6194-Chloro-3-methylphenol ........................................5925-Chloro-2-methyl-4-isothiazolin-3-one...............2352-Chlorophenol..........................................................592o-Chlorophenoxyacetic acid..........................591, 593p-Chlorophenoxyacetic acid..........................591, 593o-Chlorophenoxy proprionic acid..........................593Chlorothiazide............................................................189Chlorpheniramine ..........................275, 279, 617, 628Chlorthalidone...........................................................189Chrysene.............................................................589-591Chymotrypsinogen A ...............................................410Cimetidine ................................................325, 583, 637d-Cinchonine.....................................................266, 619Cinnamaldehyde .......................................................599Ciprofloxacin..............................................................620Citrate..........................................................................174Citric Acid................................338, 396, 581, 609-610Clindamycin ...............................................................620Clomipramine ............................................................289

Compound Index

664

COMPOUND INDEX

Clonazepam ...............................................................289Clotrimazole ...............................................................621Cobalamin (B12) .......................................................612Cocaine ..............................................................619, 627Codeine.......................................................................630Corticosterone...........................................................290Cortisone ...........................................................290, 299Cortisone acetate .....................................................290m-Cresol......................................................................590o-Cresol.............................................230-231, 584, 592p-Cresol......................................................230-231, 584Crotonaldehyde – DNPH ........................................584Cyanide .......................................................................175Cyanidin .............................................................237, 597Cyanocobalamin (B12)............................................605p-Cymene ...................................................................599Cyprodinil....................................................................594Cysteine ......................................................................396Cytidine .......................................................................568Cytochrome C ................183, 382, 370-371, 400, 403,

410, 558-560, 571, 572, 576Cytodine......................................................................564Cytosine .............................................................564, 579

DDaidzen .......................................................................266Dehydroacetic acid ..................................................232Delphinidin ........................................................237, 5972' Deoxycytidine .......................................................5682' Deoxyguanosine ..................................................5682' Deoxyinosine ........................................................568Desethylatrazine .......................................................588Desethyldesisopropylatrazine................................588Desipramine...............................................................289Dextromethorphan ...................................................628Diazepam...........................................................272, 289Dibenzo(a,h)anthracene..................................589-591Dichlorobenzidine............................................583, 5983,3-Dichlorobenzidine..............................................1832,4-Dichlorophenol ...................................................5922,3-Dichlorophenoxyacetic acid............................5912,4-Dichlorophenoxyacetic acid............................591Diclofenac.................................................235, 615, 618Dienestrol ...................................................................633Diethylstilbestrol.......................................................265Diflusinal............................................................235, 615Dihydroxy benzylamine ...........................................623Dihydroxyphenyl acetic acid..................................623Dihydroxyphenyl alanine.........................................623Diltiazen ......................................................................616Dimethoxybenzidine.................................................5983,3'-Dimethoxybenzidine ........................................583Dimethylbenzidine....................................................5832,3-Dimethyl phenol................................230-231, 5302,4-Dimethyl phenol.................................................5922,5-Dimethyl phenol................................230-231, 5303,4-Dimethyl phenol........................................231, 5841,3-Dimethyluric acid...............................................617Dimethylxanthine .....................................................276

1,7-Dimethylxanthine...............................................6173,7-Dimethylxanthine (theobromine)...................6171,3-Dinitrobenzene ...........................................586-5872,4-Dinitrophenol ......................................................5922,4-Dinitrotoluene.............................................586-5872,6-Dinitrotoluene.............................................586-587Dioctyl phthalate..............................................290, 299Diphenhydramine ...................................275, 617, 632Diphenylamine ..........................................................586Dipropyl phthalate....................................................241Dipropylthalate..........................................................250Dipyridamole..............................................................616Disopyramide.............................................................640Diuron................................................259, 587-588, 591Dopamine ..........................................................578, 623Doxepin.............................................258, 289, 635-636Doxycycline................................................................639Doxylamine ..............................................275, 279, 617Dulcitol........................................................................339

EEpinephrine................................................................623Ecgonine methylester..............................................627Econazole ...................................................................621Eletriptan ....................................................................616Epagallocatechin ......................................................603Epicatechin........................................................603, 625Epicatechin gallate..........................................603, 625Epigallocatechin........................................................625Epigallocatechin gallate.................................603, 625Estradiol ......................................................................633b -Estradiol.................................................................613Estriol ..........................................................................266Estrone........................................................................613Ethanol ...............................................................582, 610Ethinylestradiol .........................................................633Ethoprophos...............................................................594Ethyl cinnamate........................................................5992-Ethylhexyl trans-4-methoxycinnamate ............607bis-(2-Ethylhexyl) phthalate ...................................507Ethylhexyl salicylate ................................................2592-Ethylhexyl salicylate.............................................607Ethylparaben............................................189, 272, 604Eugenol .......................................................................599Excipent ......................................................................606

FFamotidine..................................................................637Fenfluramine..............................................................622Fenoprofen .................................................................622Fenuron.......................................................................259Fibrinogen..........................................................309, 392Flunitrazepam............................................................289Fluocinolone acetonide...........................................290Fluoranthene.............................................189, 589-591Fluorene.....................................................189, 589-591Fluoride ..............................................................172, 1752-Fluorobenzoic.........................................................623

3-Fluorobenzoic.........................................................623Fluorocytosine...........................................................579Folic acid....................................................605-606, 612Formaldehyde – DNPH ...........................................584Formate.......................................................................174Fructose ..................................338, 340, 600, 604, 610Fumaric Acid..............................................................581Furosemide ................................................................616

GGalactose....................................................................340Genistein ....................................................................266g-Globulin ...................................................................421Glucagon.....................................................................384Glucose ...........................338, 340-341, 600, 604, 610Glutamine ..........................................................396, 564Glutamate...................................................................175Gly3-Gly4 (Na-acetylated).............................308, 390Glyburide.....................................................................638Glycerol .......................................................................610Glyceryl Guaicolate ..................................................334Gluconate ..........................................................396, 564Glycine.......................................................389, 396, 564Guaifenesin................................................................629Guanine..............................................................564, 579Guanosine .........................................................564, 568

HHeptabarbitone .........................................................643Hexaldehyde – DNPH..............................................584Hexazinon...................................................................588Hexogen (RDX) .................................................586-587Hexyl............................................................................586Histidine.............................................................396, 564Homocyclonite ..........................................................586Homovanillic acid .....................................................623Holotransferrin ..........................................................572Hydrastine ..................................................................625Hydrochlorothiazide .................................................189Hydrocortisone........................................312, 613, 635Hydroflumethiazide ..................................................189Hydroquinone ...........................................230-231, 584Hydroxyindoleaacetic acid .....................................6232-Hydroxy-4-methoxybenzophenone ...................6074-Hydroxyropivacaine ..............................................619Hydroxyproline .................................................396, 5645- Hydroxytryptamine ..............................................623

IIbuprofen ..................................................235, 396, 618IgA................................................................................421IgG2a, I HOPC-1........................................................565IgM, MOPC-104E......................................................565Imazalil ........................................................................594Imidacloprid ...............................................................594Imipramine ...............................................289, 632, 635Indeno(1,2,3-c,d)pyrene ..................................589-591

665

COMPOUND INDEX


Indole...........................................................................6423-Indole acetic acid..................................................5933-Indole butyric acid ................................................5933-Indole proprionic acid ..........................................593Inosine.........................................................................568Insulin.......................370-371, 381-382, 462, 571-572Iodide...........................................................................172Iso-erythritol...............................................................339Isoleucine ...................................................................564Isomaltose..................................................................600Isopropanol ................................................................582Isoproturon.................................................................588

KKathon 1A ..................................................................580Kathon 1B...................................................................580Ketoprofen.........................................................235, 615Kinetin .........................................................................593Kresoxim-methyl.......................................................594

La-Lactalbumin.........................................391, 408, 578Lactate ................................................................174-175Lactic Acid ...............................................581, 338, 610Lactoglobulin A.........................................................183Lactoglobulin B.........................................................183b -Lactoglobulin (A chain) ...................391, 408, 578b -Lactoglobulin (B chain)...........391, 408, 432, 578Lactose......................................................340, 600, 602Lamotrigine ................................................................642Leucine...............................................................396, 564Leucine Enkephalin........................194, 370, 571-572Lidocaine ..................................................266, 619, 640Lincomycin.................................................................620Linuron ...............................................................259, 588Lysine .................................................................396, 564Lysozyme...............183, 370-371, 381-382, 400, 403,

410, 558-560, 571-572, 576

MMagnesium................................................................173Malate .........................................................................174Maleate.......................................................................275Maleic acid.................................................................628Malic acid...................................................................610Maltose.......................................................................600Maltotriose.................................................................340Malvidin .............................................................237, 597Mannitol ....................................................339-341, 604Mefanamic acid ........................................................241Mepivacaine ..............................................................619Metacycline ...............................................................639Metazachlor...............................................................588Met-Enkephalin........................................194, 571-572Metformin..........................................................325, 583Methabenzthiazuron................................................588Methacrolein –DHCP...............................................584

Methanol ....................................................................5823-Methaxytyrosine ...................................................623Methionine........................................................396, 564Methoxyaniline .........................................................5834-Methoxybenzenesulfonamide............................289Methoxychlor, 200 mg/L........................................507Methyl-3-aminothiophene-2-carboxylate............2892-Methyl-4,6-dinitrophenol.....................................5924,4-Methylene-bis-2-chloroaniline........................1832-Methyl-4-isothiazolin-3-one ...............................2351-Methyl naphthalene ............................................5912-Methyl naphthalene ............................................5912-Methyl-5-nitroaniline............................................183Methyl paraben..............................189, 235, 580, 604Methyl prednisolone................................................290Methyl salicylate ......................................................6021-Methylxanthine .....................................................617Metobromuron ..........................................................588Metolachlor........................................................587-588Metoprolol..................................................................613Metoxuron..................................................................588Miconazole.................................................................621Molybdate (VI) ..........................................................172Monolinuron .....................................................259, 588Monuron.....................................................................259Morphine............................................................630-631Morphine-6-glucuronide .........................................630Morphine-3-glucuronide ........................................630Myoglobin ......................370-371, 381-382, 407, 410,

421, 432, 571-572, 576

NNadolol...............................................................613, 640Naphthalene ....................................189, 241, 589-5911-Naphthol ................................................230-231, 5841-Naphthyl acetamide.............................................5931-Naphthyl acetic acid ............................................593Naphthylamine.................................................583, 598Naproxen...........................................................241, 618Neurotensin..............................................381, 571-572Niacin (B3)................................................605-606, 612Niacinamide...............................................................607Nicotinic Acid............................................................607Nifedipine ..........................................................315, 640Nimodipine........................................................315, 640Nisoldipine ........................................................315, 640Nitrate ................................................................172, 175Nitrite .................................................................172, 1752-Nitrobenzoic...........................................................6233-Nitrobenzoic...........................................................6232-Nitrophenol...................................230-231, 584, 5924-Nitrophenol...................................230-231, 584, 5922-Nitrotoluene ...................................................586-5873-Nitrotoluene ...................................................586-5874-Nitrotoluene ...................................................586-587Noradrenaline............................................................578Nordiazepam..............................................................289Nordoxepin.................................................................289Norepinephrine .........................................................623

Norethindrone...........................................................633Norethindrone acetate............................................613Normorphine..............................................................631Nortriptyline............................250, 258, 289, 635-637cis-10-OH-Nortriptyline ...........................................637trans-10-OH-Nortriptyline.......................................637Norvaline ...........................................................396, 564

OOctogen (HMX).........................................................587Octylmethoxycinnamate .........................................250Oleoylethanolamide (OEA)............................328, 614Orotic Acid .................................................................568Ovalbumin ......................................381, 407, 412, 421,

558-560, 572, 576Oxalate ........................................................................174Oxalic acid.........................................................338, 389Oxybenzone.......................................................250, 259Oxytetracycline..........................................................639Oxytocin......................................................................462

PPadimate-O .......................................................259, 607Palatinose...................................................................600Palmatine ...................................................................625Palmitoylethanolamide...................................236, 614Pantothenic acid..............................................605, 612Parvalbumin...............................................................371Penconazole ..............................................................594Pencycuron ................................................................259Pentachlorophenol ...................................................592iso-Pentane................................................................565Pentylparaben ...........................................................189Peonidin.............................................................237, 597Perphenazine.............................................................632Perylene......................................................................507Petunidin ...........................................................237, 597Phenacetin ......................................235, 615, 618, 622Phenanthrene...........................................189, 589-591Phenobarbitone.........................................................643Phenol.......................................................231, 240, 249,

299, 584, 592Phenoxyacetic acid..................................................5912-Phenoxyethanol............................................235, 580Phentermine ..............................................................622Phenylalanine (PHE) ..............................396, 564, 599Phenylbutazone ........................................................622Phenylephrine ...........................................................334Phosphate ..........................................................174-175Phthalic acid ..............................................................623p-hydroxybenzoic acid.............................................232Picric acid...................................................................586Pindolol .....................................................613, 640, 642Pioglitazone ...............................................................616Pirenzepine ................................................................637Piroxicam...........................................................235, 615Poly-DL-alanine.........................................................425Potassium...................................................................173

666

COMPOUND INDEX

Prednisolone.....................................................290, 632Prednisolone acetate...............................................290Procainamide....................................................616, 640Procaine....................................................266, 619, 640Progesterone ....................................................613, 638Promethazine.............................................................632Prometon....................................................................587Prométryne........................................................587, 591Propanil..............................................................587, 591n-Propanol..................................................................582Propanolol ..................................................................636Propazine...................................................587-588, 591Propionaldehyde – DNPH ......................................584Propoxur .....................................................................594Propranolol......................................241, 613, 636, 640Propylparaben ..................................................189, 604Protriptyline..............................................396, 564, 632Pseudoephedrine....................................275, 617, 628Pymetrozine ...............................................................594Pyrene .................................................................589-591Pyridine ..............................................................249, 389Pyridoxine...........................................................605-607Pyridoxyl phosphate (B6) .......................................612Pyrilamine...................................................................334Pyroglutamate ...........................................................174Pyruvate......................................................................174

QQuercetin ....................................................................266

RRaffinose...................................................340, 600, 604Ranitidine...........................................................325, 583Reserpine...........................................................290, 299Resorcinol..................................................230-231, 584Retinol .........................................................................605Retinol acetate..........................................................605Retinol palmitate ......................................................605Rhamnose ..................................................................600Riboflavin (B2)..........................................605-606, 612 Ribonuclease (RNase)...................371, 381, 571-572Ribonuclease A.......................370, 400, 403, 425-426,

558-560, 571-572, 576Ribose..........................................................................600Ropivacaine................................................................619

SSaccharin....................................................................232Saccharose ................................................................600Salicylic acid ...................................235, 290, 618, 621Sarcosine...........................................................396, 564Scopolamine .....................................................275, 617Sebutylazine...............................................................588Selenate......................................................................175Serine .................................................................396, 564Simazine .............................................................587-588Sodium........................................................................173

Sorbic acid................................................290, 609, 621Sorbitol.......................................................338-341, 604Stachyose..........................................................340, 604Succinate....................................................................174Succinic Acid...........................................338, 581, 610Sucrose ....................................338, 340-341, 600, 604Sulfachloropyridazine ..............................................616Sulfadiazine......................................249, 616, 640-641Sulfadimethoxine.............................................616, 641Sulfamerazine..................................249, 616, 640-641Sulfamethazine ........................................616, 640-641Sulfamethizole..................................................616, 641Sulfamethoxazole ..........................249, 258, 616, 632Sulfamethoxypyridazine..........................................616Sulfanilamide............................................249, 640-641Sulfanilic acid ............................................................641Sulfapyridine..............................................................616Sulfate ........................................................172, 174-175Sulfathiazole ............................................249, 616, 640Sulfisoxazole..............................................................641Sulfmethazine............................................................249Sulfur ...........................................................................507Sulindac .............................................................235, 615

TTalbarbitone ...............................................................643Tartarate......................................................................175Tartaric acid.......................................................338, 610Tebuthiuron ................................................................587Terbutylazine..............................................................588Terphenyl-d14 ...........................................................591o-Terphenyl.................................................................299Testosterone .....................................................312, 613Tetracaine..........................................................266, 6192,3,4,6-Tetrachlorophenol........................................592Tetryl ....................................................................586-587Theobromine............................................276, 316, 608Theophylline ............................................276, 316, 334Thiabendazole ...........................................................594Thiamine pyrophosphate (TPP) ............................594Thiamine (B1)...................................................607, 612Thiocyanate ...............................................................172Thiosulfate .................................................................172Thiourea.............................................................189, 590Threonine (THR) ..............................................396, 564Thymidine...................................................................564Thymine .............................................................564, 579Thymol ........................................................................602Thyroglobulin...................................421, 425-426, 432a-Tocopherol.....................................................605, 608b-Tocopherol ..............................................................608g-Tocopherol......................................................605, 608Tocopherol acetate...................................................605o-Tolidine.....................................................................598Tolmetin ...........................................235, 615, 618, 622m-Tolualdehyde – DNPH.........................................584Toluene..............................................240, 299, 589-591m-Toluic.......................................................................623m-Toluidine.................................................................585

o-Toluidine ................................................183, 583, 598Trehalulose.................................................................600Triamcinolone ...................................................290, 635Triamcinolone acetonide ........................................2902,4,6-Trichlorophenol................................................5922,4,5-Trichlorophenoxyacetic acid.........................5913,4,5-Trichlorophenoxyacetic acid.........................5932,4,5-Trichlorophenoxypropionic acid (Silvex)....5913,4,5-Trichlorophenoxyproprionic acid .................593Triflupromazine..........................................................632Trimipramine ...........................258, 289, 632, 635-6361,3,5-Trinitrobenzene........................................586-5872,4,6-Trinitrotoluene .........................................586-587Tripelennamine..........................................................632Triphenylene...............................................................299Triprolidine................................................275, 279, 617Tryptophan (TRP)....................................396, 459, 564Tyrosine (TYR) .........................................396, 459, 564Tébuthiuron................................................................591

UUracil...............240-241, 258, 299, 425-426, 564, 579Uridine................................................................564, 568

VValeraldehyde – DNPH ...........................................584Valine..................................................................396, 564Valine3-Glyine4 (Na-acetylated) .................308, 390Valine3-Valine4 (Na-acetylated)..................308, 390Valine-tyrosine-valine ..............................................572Vitamin A....................................................................605Vitamin B12 ...............................................................421Vitamin C...................................................605-606, 609Vitamin D2..................................................................605Vitamin D3..................................................................605Vitamin E (a-VE)........................................................605

WWarfarin .....................................................................640

XXanthosine-5’-monophosphate (XMP) ...............568Xylitol...........................................................................339Xylose..........................................................................600

667

ORDERING INFORMATION


Ordering InformationEasy Ordering Terms and Conditions

Agilent Technologies specializes in fast delivery. In the US, if you call before 2 PM EST, we will ship yourorder that day. You may also request overnight express delivery before 6 PM EST and you will have yourorder the next day. Volume discounts on a variety of individual products are offered when the entire quantityis shipped to one address at one time.

A shipping and handling fee will be added to your order unless the purchase is over $2000 US for ordersplace online or over $4000 for orders place via phone. Special shipping (i.e., overnight in the US) isavailable in most regions at an additional cost.

Agilent is required to collect all state and local sales taxes unless the buyer's tax-exempt certificate is on filewith Agilent Technologies. Please be prepared to provide a copy if it is not on file, when placing your order.

Please check with your Agilent Customer Service Representative, local Authorized Distributor, or the Agilentwebsite for current prices, special offers, promotions and discounts when placing your order.

Satisfaction GuaranteedIf you are not satisfied with your Agilent product within the first 60 days, you may return your purchase in itsoriginal condition for a full refund or credit. A return policy statement is included in every Agilent shipmentand posted under Product Information on the website. In the US and Canada, please call for a ReturnAuthorization form and return instructions at 1-800-227-9770. If your Agilent product was purchased froma distributor, please contact the distributor.

Shipping DamagesIf items are damages in transit, please follow the instructions below:

• If a shipment is visibly damaged upon arrival, do not accept it until the person making the delivery hasendorsed the bill of lading with statement for the extent of the damage.

• If any damage is found after unpacking, retain all cartons and inner packaging and immediatelyrequest an inspection from the carrier.

• Notify the Agilent Customer Contact Center at 1-800-227-9770 about the damaged shipment so thatwe can make the appropriate sales adjustment and/or provide you with return instructions (Sales ordernumber, product number and quantity damaged will be needed).

Discounts and Delivery

668


Easy Ways To Order• Phone: 1-800-227-9770 (option 1, 1) in the US and Canada – Mon-Fri, 8AM to 8PM EST• Fax: 1-302-633-8901 in the US• Email: [email protected] in the US and Canada• Online: www.agilent.com/chem in the US and Canada

Payment Options• In the US, Visa, MasterCard, Discover and American Express are accepted with a minimum order of$20 (not applicable in all countries).

• Email [email protected] to make an electronic payment using the ACH/EFT (Automated ClearingHouse/Electronic Funds Transfer) method.

• Establish a charge account through your Agilent Customer Service Representative or Your Local Agilentsales office. An account number will be assigned to you for charging your purchases. Payment termsare net 30 days from the invoice date. All orders are subject to credit approval.

We will be happy to supply a price quote via, phone, email or fax if you need it in writing.

WarrantiesAll Agilent Technologies products in this catalog are designed and manufactured to stringent standardsunder the Agilent quality system registered to ISO 9001. At Agilent, we back every product with a 90-daywarranty and a money-back guarantee. If Agilent receives notice of defects during the warranty period.Agilent shall, at its option, either repair or replace products which prove to be defective. If Agilent is unable,within a reasonable time, to repair or replace any product to a condition as warranted, the buyer shall beentitled to a refund of the purchase price upon return of the product to Agilent. The warranty period foreach product begins on the day of shipment.

This warranty shall not apply to any defect, failure, or damage caused by improper use or improper orinadequate maintenance or care. This warranty is exclusive and no other warranty, whether written or oral,is expressed or implied. Agilent specifically disclaims the implied warranties of merchantability and fitnessfor particular purposes. The remedies provided herein are the buyer's sole and exclusive remedies. In noevent shall Agilent be liable for direct, indirect, special, incidental, or consequential damages (including lossof profits) whether based on contract, tort, or any other legal theory.

669



Agilent Technologies Order Form Agilent Technologies

Order Date Purchase Order or Credit Card Number & Expiration

Shipping Address

Description Quantity Price Total CostPart Number

Billing Address

If No, please provide Certificate #

TaxableY or N?

Yes No

Name:

Title:

Phone:

Company:

Fax:

Email:

Subtotal:Special Instructions:

For Assistance: Please call the Agilent Technologies Customer Contact Center at 1-800-227-9770 (U.S. and Canada)Email Node: [email protected] Number: 302-633-8901 U.S. and CanadaNote: 1. All pricing, tax, discount, and availability information is subject to verification by Agilent Technologies. 2. Shipping and handling is free for orders over $2000 US.

Tax:

Company:

Street:

Room/Bldg/Dept:

City:

State/Province/Country:

Zip/Postal Code:

Deliver to:

Total:

Outside the U.S. and Canada, please contact your local Agilent office or Authorized Distributor when ordering.

670




Shipping Address


Billing Address


TaxableY or N?

Yes No

Name:

Title:

Phone:

Company:

Fax:

Email:



Tax:

Company:

Street:

Room/Bldg/Dept:

City:


Zip/Postal Code:

Deliver to:

Total:


671





Shipping Address


Billing Address


TaxableY or N?

Yes No

Name:

Title:

Phone:

Company:

Fax:

Email:



Tax:

Company:

Street:

Room/Bldg/Dept:

City:


Zip/Postal Code:

Deliver to:

Total:


672

NOTES

Your Essential Resource for Columns & SuppliesLC & LC/MS

For more information

Buy online:www.agilent.com/chem/store

Contact us:www.agilent.com/chem/contactus

Scan the QR codewith your smartphonefor more information

THE ESSENTIAL CHROMATOGRAPHY & SPECTROSCOPY CATALOG

LC AND LC/MSThis information is subject to change without notice.

© Agilent Technologies, Inc. 2012Printed in Canada October 31, 20125991-1059EN

thesential c buy online: hromato contact us: gr phy s this ... columns catalog.pdf · zorbax...

Documents